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Generic macrocrystalline nitrofurantoin

No pharmacy we check posts a price for it.

  1. Ask your pharmacy for the cash price of generic macrocrystalline nitrofurantoin.Find pharmacies near you 
  2. Ask one or two other pharmacies too. Cash prices for the same generic can differ a lot from store to store.

A regular generic has the same active ingredient as Macrodantin, and the FDA requires it to work the same way.

Compare every option

Question
Brand nameMacrodantin
Authorized genericmacrocrystalline nitrofurantoin
Regular genericmacrocrystalline nitrofurantoin
What you’d pay
Not soldNo longer sold
Not soldNo longer sold
Cash priceAsk the pharmacy
Same as Macrodantin?
–
–
Same active ingredientFillers and dyes can differ

Brand nameNot sold

Macrodantin itself isn’t sold as a prescription anymore. Its generic versions, if any, are in the other tabs.

See the regular generic →

Authorized genericNot sold now

An authorized generic of Macrodantin was sold before, but it isn’t sold now. Ask your pharmacist whether a regular generic (macrocrystalline nitrofurantoin) is available.

Source: FDA, updated October 30, 2026

Regular genericWho makes it

7 companies sell a generic of Macrodantin that the FDA rates a substitute. A pharmacy fills whichever one it stocks. To get a certain maker, ask for it by name; most pharmacies can order it in a day or two.

  • Alembic Pharmaceuticals25 mg, 50 mg, 100 mg

    Has lactose · Has dyes: D&C Red No. 33, D&C Yellow No. 10

    How it looks, what’s in it, NDCs

    25 mg White, capsule, 14 mm, marked “A219”

    PackageNDC
    Bottle of 10062332-389-31
    Bottle of 100062332-389-91

    50 mg Yellow and white, capsule, 16 mm, marked “A220”

    PackageNDC
    Bottle of 10062332-390-31
    Bottle of 100062332-390-91

    100 mg Yellow, capsule, 18 mm, marked “A221”

    PackageNDC
    Bottle of 10062332-391-31
    Bottle of 100062332-391-91

    Inactive ingredients: lactose monohydrate, starch, corn, talc, gelatin, titanium dioxide, shellac, propylene glycol, potassium hydroxide, ferrosoferric oxide, D&C Red No. 33, D&C Yellow No. 10

    FDA label

  • Amneal Pharmaceuticals50 mg, 100 mg

    Has lactose · Has dyes: D&C Red No. 33, D&C Yellow No. 10, FD&C Blue No. 1, FD&C Blue No. 2, FD&C Red No. 40 · Made by Impax Laboratories

    How it looks, what’s in it, NDCs

    50 mg Pink and white, capsule, 16 mm, marked “Z / Zenith / 50mg / 2130”

    PackageNDC
    Bottle of 1000115-1643-01
    Bottle of 10000115-1643-03

    100 mg Pink, capsule, 18 mm, marked “Z / Zenith / 100mg / 2131”

    PackageNDC
    Bottle of 1000115-1645-01
    Bottle of 10000115-1645-03

    Inactive ingredients: starch, corn, ferrosoferric oxide, D&C Yellow No. 10, aluminum oxide, FD&C Blue No. 1, FD&C Blue No. 2, indigotindisulfonate sodium, FD&C Red No. 40, propylene glycol, shellac, gelatin, lactose monohydrate, talc, titanium dioxide, D&C Red No. 33

    FDA label

  • Aurobindo Pharma50 mg, 100 mg

    Has lactose

    How it looks, what’s in it, NDCs

    50 mg Light brown opaque, capsule, 18 mm, marked “NT50”

    PackageNDC
    Bottle of 10059651-753-01

    100 mg Gray opaque, capsule, 18 mm, marked “NT100”

    PackageNDC
    Bottle of 10059651-795-01

    Inactive ingredients: silicon dioxide, starch, corn, gelatin, lactose monohydrate, magnesium stearate, ferric oxide red, sodium lauryl sulfate, titanium dioxide, ferric oxide yellow, ferrosoferric oxide, potassium hydroxide, propylene glycol, shellac, talc

    FDA label

  • BluePoint Laboratories25 mg, 50 mg, 100 mg

    Has lactose · Has dyes: FD&C Blue No. 1, FD&C Red No. 3 · Made by Mankind Pharma

    How it looks, what’s in it, NDCs

    25 mg Opaque cap and body, capsule, 11 mm, marked “LS / 410”

    PackageNDC
    Bottle of 10068001-603-00

    50 mg Opaque cap and opaque body, capsule, 16 mm, marked “LS / 411”

    PackageNDC
    Bottle of 10068001-604-00

    100 mg Opaque cap and body, capsule, 18 mm, marked “LS / 412”

    PackageNDC
    Bottle of 10068001-605-00

    Inactive ingredients: starch, corn, talc, titanium dioxide, gelatin, shellac, ferrosoferric oxide, potassium hydroxide, lactose monohydrate, FD&C Red No. 3, FD&C Blue No. 1

    FDA label

  • Lupin Pharmaceuticals50 mg, 100 mg

    Has lactose · Made by Novel Laboratories

    How it looks, what’s in it, NDCs

    50 mg Pink, capsule, 16 mm, marked “50mg / Novel”

    PackageNDC
    Bottle of 10043386-641-01

    100 mg Gray, capsule, 18 mm, marked “100mg / Novel”

    PackageNDC
    Bottle of 10043386-642-01

    Inactive ingredients: lactose monohydrate, starch, corn, talc, ferric oxide red, ferric oxide yellow, shellac, potassium hydroxide, titanium dioxide, gelatin, ferrosoferric oxide, propylene glycol

    FDA label

  • NorthStar Rx25 mg, 50 mg, 100 mg

    Has lactose · Has dyes: FD&C Blue No. 1, FD&C Red No. 3 · Made by Mankind Pharma

    How it looks, what’s in it, NDCs

    25 mg Opaque cap and body, capsule, 11 mm, marked “LS / 410”

    PackageNDC
    Bottle of 10072603-182-01

    50 mg Opaque cap and opaque body, capsule, 16 mm, marked “LS / 411”

    PackageNDC
    Bottle of 10072603-183-01

    100 mg Opaque cap and body, capsule, 18 mm, marked “LS / 412”

    PackageNDC
    Bottle of 10072603-184-01

    Inactive ingredients: lactose monohydrate, starch, corn, talc, titanium dioxide, gelatin, shellac, ferrosoferric oxide, potassium hydroxide, FD&C Red No. 3, FD&C Blue No. 1

    FDA label

  • Zydus Lifesciences50 mg

    Has lactose · Has dyes: FD&C Blue No. 1, FD&C Red No. 3

    How it looks, what’s in it, NDCs

    50 mg Blue opaque and white opaque, capsule, 16 mm, marked “559”

    PackageNDC
    Bottle of 10068382-559-01
    Carton of 10068382-559-30
    Bottle of 100068382-559-10

    Inactive ingredients: FD&C Blue No. 1, FD&C Red No. 3, gelatin, lactose monohydrate, magnesium stearate, sodium lauryl sulfate, starch, corn, talc, titanium dioxide

    FDA label

Who sells it: FDA and Medicaid records, updated weekly. Each maker’s page, card and program is from its own site.

What it’s used for

What the FDA label says

INDICATIONS AND USAGE:

Macrodantin is specifically indicated for the treatment of urinary tract infections when due to susceptible strains of Escherichia coli, enterococci, Staphylococcus aureus, and certain susceptible strains of Klebsiella and Enterobacter species.

Nitrofurantoin is not indicated for the treatment of pyelonephritis or perinephric abscesses.

To reduce the development of drug-resistant bacteria and maintain the effectiveness of Macrodantin and other antibacterial drugs, Macrodantin should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy.

Nitrofurantoins lack the broader tissue distribution of other therapeutic agents approved for urinary tract infections. Consequently, many patients who are treated with Macrodantin are predisposed to persistence or reappearance of bacteriuria. Urine specimens for culture and susceptibility testing should be obtained before and after completion of therapy. If persistence or reappearance of bacteriuria occurs after treatment with Macrodantin, other therapeutic agents with broader tissue distribution should be selected. In considering the use of Macrodantin, lower eradication rates should be balanced against the increased potential for systemic toxicity and for the development of antimicrobial resistance when agents with broader tissue distribution are utilized.

Source: the FDA label for Macrodantin (Procter & Gamble Pharmaceuticals), March 23, 2009. Full label on DailyMed