NDC codes

FDA NDC Directory
Product NDC (as listed)76420-884Labeler and product segments. Claims need a package NDC.
Product NDC at billing width76420-0884Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
76420-884-0076420088400764200884001000 CAPSULE in 1 BOTTLE (76420-884-00)Marketed from Dec 17, 2024
76420-884-017642008840176420088401100 CAPSULE in 1 BOTTLE (76420-884-01)Marketed from Dec 17, 2024
76420-884-0776420088407764200884077 CAPSULE in 1 BOTTLE (76420-884-07)Marketed from Dec 17, 2024
76420-884-10764200884107642008841010 CAPSULE in 1 BOTTLE (76420-884-10)Marketed from Jan 9, 2025
76420-884-12764200884127642008841212 CAPSULE in 1 BOTTLE (76420-884-12)Marketed from Dec 17, 2024
76420-884-14764200884147642008841414 CAPSULE in 1 BOTTLE (76420-884-14)Marketed from Dec 17, 2024
76420-884-20764200884207642008842020 CAPSULE in 1 BOTTLE (76420-884-20)Marketed from Dec 17, 2024
76420-884-28764200884287642008842828 CAPSULE in 1 BOTTLE (76420-884-28)Marketed from Dec 17, 2024
76420-884-30764200884307642008843030 CAPSULE in 1 BOTTLE (76420-884-30)Marketed from Dec 17, 2024
76420-884-60764200884607642008846060 CAPSULE in 1 BOTTLE (76420-884-60)Marketed from Dec 17, 2024
76420-884-90764200884907642008849090 CAPSULE in 1 BOTTLE (76420-884-90)Marketed from Dec 17, 2024

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Generic name (nonproprietary)
nitrofurantoin (monohydrate/macrocrystals)
Active ingredients
Nitrofurantoin monohydrate — 75 mg/1Nitrofurantoin — 25 mg/1
Dosage form
Capsule
Route
Oral
Labeler
Asclemed USA, Inc.NDC labeler code 76420
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 211013
Marketing start
Listing expires
Other FDA classes
Nitrofurans (Chemical structure)Nitrofurans (Chemical structure)
Identifiers
Product ID 76420-884_2b480a86-eebf-c37e-e063-6394a90ae54bSPL ID 2b480a86-eebf-c37e-e063-6394a90ae54bSPL set ID ee3f300a-d6d3-49c4-bd60-425f04d30b88RxCUI 1648755UNII E1QI2CQQ1I, 927AH8112L
Pharmacologic class
Nitrofuran Antibacterial

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N476420088400 followed by a unit qualifier and the quantity

Package 76420-0884-00. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective .

Indications (excerpt from the label)

INDICATIONS AND USAGE Nitrofurantoin capsules (monohydrate/macrocrystals) are indicated only for the treatment of acute uncomplicated urinary tract infections (acute cystitis) caused by susceptible strains of Escherichia coli or Staphylococcus saprophyticus. 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 nitrofurantoin capsule (monohydrate/macrocrystals) and other antibacterial drugs, nitrofurantoin capsule (monohydrate/macrocrystals) should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 76420-884

What is NDC 76420-884?
76420-884 is the product NDC for NITROFURANTOIN (monohydrate/macrocrystals), Nitrofurantoin monohydrate 75 mg/1; Nitrofurantoin 25 mg/1 capsule, listed with the FDA by Asclemed USA, Inc.. It has 11 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
NITROFURANTOIN (monohydrate/macrocrystals).
What is the active ingredient?
Nitrofurantoin monohydrate, Nitrofurantoin.
Who is the labeler?
Asclemed USA, Inc., NDC labeler code 76420. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for NITROFURANTOIN (monohydrate/macrocrystals)?
32 other product NDCs are listed under this name. See all NITROFURANTOIN (monohydrate/macrocrystals) NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other NITROFURANTOIN (monohydrate/macrocrystals) NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Nitrofurantoin (monohydrate/macrocrystals)Nitrofurantoin monohydrate 75 mg/1; Nitrofurantoin 25 mg/1CapsuleOralCoupler LLC67046-119867046-1198-03
Nitrofurantoin (monohydrate/macrocrystals)Nitrofurantoin monohydrate 75 mg/1; Nitrofurantoin 25 mg/1CapsuleOralCoupler LLC67046-127167046-1271-03
Nitrofurantoin (Monohydrate/Macrocrystals)Nitrofurantoin 25 mg/1; Nitrofurantoin monohydrate 75 mg/1CapsuleOralCreekwood Pharmaceuticals LLC82619-14782619-0147-0182619-0147-0282619-0147-03
Nitrofurantoin (monohydrate/macrocrystals)Nitrofurantoin monohydrate 75 mg/1; Nitrofurantoin 25 mg/1CapsuleOralMajor Pharmaceuticals0904-757100904-7571-61
Nitrofurantoin (monohydrate/macrocrystals)Nitrofurantoin monohydrate 75 mg/1; Nitrofurantoin 25 mg/1CapsuleOralREMEDYREPACK INC.70518-435870518-4358-00
NITROFURANTOIN (monohydrate/macrocrystals)Nitrofurantoin monohydrate 75 mg/1; Nitrofurantoin 25 mg/1CapsuleOralNorthwind Health Company, LLC82868-06582868-0065-1082868-0065-1482868-0065-20
Nitrofurantoin (monohydrate/macrocrystals)Nitrofurantoin monohydrate 75 mg/1; Nitrofurantoin 25 mg/1CapsuleOralREMEDYREPACK INC.70518-402670518-4026-0070518-4026-0170518-4026-02+1 more
Nitrofurantoin (monohydrate/macrocrystals)Nitrofurantoin monohydrate 75 mg/1; Nitrofurantoin 25 mg/1CapsuleOralPreferred Pharmaceuticals Inc.68788-857168788-8571-0068788-8571-01
Nitrofurantoin (monohydrate/macrocrystals)Nitrofurantoin monohydrate 75 mg/1; Nitrofurantoin 25 mg/1CapsuleOralNorthStar RxLLC72603-19672603-0196-01
Nitrofurantoin (monohydrate/macrocrystals)Nitrofurantoin monohydrate 75 mg/1; Nitrofurantoin 25 mg/1CapsuleOralBluePoint Laboratories68001-60668001-0606-00

All 33 NITROFURANTOIN (monohydrate/macrocrystals) NDCs

Other NDCs under ANDA 211013

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 211013
ProductStrengthForm · routeLabelerProduct NDC
Nitrofurantoinnitrofurantoin (monohydrate/macrocrystals)Nitrofurantoin monohydrate 75 mg/1; Nitrofurantoin 25 mg/1CapsuleOralA-S Medication Solutions50090-6664
Nitrofurantoinnitrofurantoin (monohydrate/macrocrystals)Nitrofurantoin monohydrate 75 mg/1; Nitrofurantoin 25 mg/1CapsuleOralA-S Medication Solutions50090-6750
NITROFURANTOIN (monohydrate/macrocrystals)Nitrofurantoin monohydrate 75 mg/1; Nitrofurantoin 25 mg/1CapsuleOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8531
NITROFURANTOIN (monohydrate/macrocrystals)Nitrofurantoin monohydrate 75 mg/1; Nitrofurantoin 25 mg/1CapsuleOralQPharma, Inc.42708-184
NITROFURANTOIN (monohydrate/macrocrystals)Nitrofurantoin monohydrate 75 mg/1; Nitrofurantoin 25 mg/1CapsuleOralJubilant Cadista Pharmaceuticals Inc.59746-762
NITROFURANTOIN (monohydrate/macrocrystals)Nitrofurantoin monohydrate 75 mg/1; Nitrofurantoin 25 mg/1CapsuleOralRedpharm Drug67296-2180
NITROFURANTOIN (monohydrate/macrocrystals)Nitrofurantoin monohydrate 75 mg/1; Nitrofurantoin 25 mg/1CapsuleOralNorthwind Health Company, LLC82868-065

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