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
Generic name: macrocrystalline nitrofurantoin
Used for: Urinary tract infections
Ask for the cash price
Generic macrocrystalline nitrofurantoin
No pharmacy we check posts a price for it.
A regular generic has the same active ingredient as Macrodantin, and the FDA requires it to work the same way.
Details for each option
Macrodantin itself isn’t sold as a prescription anymore. Its generic versions, if any, are in the other tabs.
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
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.
Has lactose · Has dyes: D&C Red No. 33, D&C Yellow No. 10
25 mg White, capsule, 14 mm, marked “A219”
| Package | NDC |
|---|---|
| Bottle of 100 | 62332-389-31 |
| Bottle of 1000 | 62332-389-91 |
50 mg Yellow and white, capsule, 16 mm, marked “A220”
| Package | NDC |
|---|---|
| Bottle of 100 | 62332-390-31 |
| Bottle of 1000 | 62332-390-91 |
100 mg Yellow, capsule, 18 mm, marked “A221”
| Package | NDC |
|---|---|
| Bottle of 100 | 62332-391-31 |
| Bottle of 1000 | 62332-391-91 |
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
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
50 mg Pink and white, capsule, 16 mm, marked “Z / Zenith / 50mg / 2130”
| Package | NDC |
|---|---|
| Bottle of 100 | 0115-1643-01 |
| Bottle of 1000 | 0115-1643-03 |
100 mg Pink, capsule, 18 mm, marked “Z / Zenith / 100mg / 2131”
| Package | NDC |
|---|---|
| Bottle of 100 | 0115-1645-01 |
| Bottle of 1000 | 0115-1645-03 |
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
Has lactose
50 mg Light brown opaque, capsule, 18 mm, marked “NT50”
| Package | NDC |
|---|---|
| Bottle of 100 | 59651-753-01 |
100 mg Gray opaque, capsule, 18 mm, marked “NT100”
| Package | NDC |
|---|---|
| Bottle of 100 | 59651-795-01 |
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
Has lactose · Has dyes: FD&C Blue No. 1, FD&C Red No. 3 · Made by Mankind Pharma
25 mg Opaque cap and body, capsule, 11 mm, marked “LS / 410”
| Package | NDC |
|---|---|
| Bottle of 100 | 68001-603-00 |
50 mg Opaque cap and opaque body, capsule, 16 mm, marked “LS / 411”
| Package | NDC |
|---|---|
| Bottle of 100 | 68001-604-00 |
100 mg Opaque cap and body, capsule, 18 mm, marked “LS / 412”
| Package | NDC |
|---|---|
| Bottle of 100 | 68001-605-00 |
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
Has lactose · Made by Novel Laboratories
50 mg Pink, capsule, 16 mm, marked “50mg / Novel”
| Package | NDC |
|---|---|
| Bottle of 100 | 43386-641-01 |
100 mg Gray, capsule, 18 mm, marked “100mg / Novel”
| Package | NDC |
|---|---|
| Bottle of 100 | 43386-642-01 |
Inactive ingredients: lactose monohydrate, starch, corn, talc, ferric oxide red, ferric oxide yellow, shellac, potassium hydroxide, titanium dioxide, gelatin, ferrosoferric oxide, propylene glycol
Has lactose · Has dyes: FD&C Blue No. 1, FD&C Red No. 3 · Made by Mankind Pharma
25 mg Opaque cap and body, capsule, 11 mm, marked “LS / 410”
| Package | NDC |
|---|---|
| Bottle of 100 | 72603-182-01 |
50 mg Opaque cap and opaque body, capsule, 16 mm, marked “LS / 411”
| Package | NDC |
|---|---|
| Bottle of 100 | 72603-183-01 |
100 mg Opaque cap and body, capsule, 18 mm, marked “LS / 412”
| Package | NDC |
|---|---|
| Bottle of 100 | 72603-184-01 |
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
Has lactose · Has dyes: FD&C Blue No. 1, FD&C Red No. 3
50 mg Blue opaque and white opaque, capsule, 16 mm, marked “559”
| Package | NDC |
|---|---|
| Bottle of 100 | 68382-559-01 |
| Carton of 100 | 68382-559-30 |
| Bottle of 1000 | 68382-559-10 |
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
Who sells it: FDA and Medicaid records, updated weekly. Each maker’s page, card and program is from its own site.
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
Prices change: confirm with the pharmacy before you fill. drugalt.com/drug/macrodantin/