NDC codes

FDA NDC Directory
Product NDC (as listed)71335-2255Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-2255Add 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
71335-2255-1713352255017133522550140 CAPSULE in 1 BOTTLE (71335-2255-1)Marketed from Oct 2, 2023
71335-2255-2713352255027133522550228 CAPSULE in 1 BOTTLE (71335-2255-2)Marketed from Oct 2, 2023
71335-2255-3713352255037133522550330 CAPSULE in 1 BOTTLE (71335-2255-3)Marketed from Oct 2, 2023
71335-2255-4713352255047133522550420 CAPSULE in 1 BOTTLE (71335-2255-4)Marketed from Oct 2, 2023
71335-2255-5713352255057133522550514 CAPSULE in 1 BOTTLE (71335-2255-5)Marketed from Oct 2, 2023
71335-2255-6713352255067133522550610 CAPSULE in 1 BOTTLE (71335-2255-6)Marketed from Oct 2, 2023
71335-2255-7713352255077133522550712 CAPSULE in 1 BOTTLE (71335-2255-7)Marketed from Oct 2, 2023
71335-2255-8713352255087133522550890 CAPSULE in 1 BOTTLE (71335-2255-8)Marketed from Oct 2, 2023
71335-2255-971335225509713352255096 CAPSULE in 1 BOTTLE (71335-2255-9)Marketed from Oct 2, 2023

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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

Brand name (proprietary)
Nitrofurantoin
Generic name (nonproprietary)
nitrofurantoin
Active ingredients
Nitrofurantoin — 25 mg/1Nitrofurantoin monohydrate — 75 mg/1
Dosage form
Capsule
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 71335
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 208516
Marketing start
Listing expires
Other FDA classes
Nitrofurans (Chemical structure)Nitrofurans (Chemical structure)
Identifiers
Product ID 71335-2255_f3e9bbf9-ad43-4ce6-aca0-d7ed0a4499fcSPL ID f3e9bbf9-ad43-4ce6-aca0-d7ed0a4499fcSPL set ID b807bd48-71ab-4578-b1d7-4d3260bf6c75RxCUI 1648755UNII 927AH8112L, E1QI2CQQ1I
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

N471335225501 followed by a unit qualifier and the quantity

Package 71335-2255-01. 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, USP (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 Capsules, USP (monohydrate/macrocrystals) and other antibacterial drugs, Nitrofurantoin Capsules, USP (monohydrate/macrocrystals) should be used only to treat or prevent infections that are proven or strongly suspected to be caused by sus…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-2255

What is NDC 71335-2255?
71335-2255 is the product NDC for Nitrofurantoin, Nitrofurantoin 25 mg/1; Nitrofurantoin monohydrate 75 mg/1 capsule, listed with the FDA by Bryant Ranch Prepack. It has 9 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Nitrofurantoin.
What is the active ingredient?
Nitrofurantoin, Nitrofurantoin monohydrate.
Who is the labeler?
Bryant Ranch Prepack, NDC labeler code 71335. 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?
43 other product NDCs are listed under this name. See all Nitrofurantoin 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 NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
NitrofurantoinNitrofurantoin 25 mg/5mLSuspensionOralCamber Pharmaceuticals, Inc.31722-49131722-0491-23
NitrofurantoinNitrofurantoin 25 mg/5mLFor suspensionOralSomerset Therapeutics, LLC70069-82970069-0829-01
NitrofurantoinNitrofurantoin 100 mg/1CapsuleOralREMEDYREPACK INC.70518-424470518-4244-00
NitrofurantoinNitrofurantoin 25 mg/5mLSuspensionOralBiocon Pharma Inc70377-11870377-0118-31
NitrofurantoinNitrofurantoin 100 mg/1CapsuleOralMicro Labs Limited42571-39342571-0393-0142571-0393-0542571-0393-90
NitrofurantoinNitrofurantoin 50 mg/5mLSuspensionOralRising Pharma Holdings, Inc.16571-88816571-0888-06
nitrofurantoinnitrofurantoin macrocrystalsNitrofurantoin 100 mg/1CapsuleOralA-S Medication Solutions50090-721750090-7217-0050090-7217-0250090-7217-03
NitrofurantoinNitrofurantoin 25 mg/1; Nitrofurantoin monohydrate 75 mg/1CapsuleOralSt. Mary's Medical Park Pharmacy60760-85360760-0853-14
Nitrofurantoinnitrofurantoin (monohydrate/macrocrystals)Nitrofurantoin monohydrate 75 mg/1; Nitrofurantoin 25 mg/1CapsuleOralNuCare Pharmaceuticals,Inc.68071-356968071-3569-0168071-3569-0268071-3569-04
NitrofurantoinNitrofurantoin monohydrate 25 mg/5mLSuspensionOralAurobindo Pharma Limited59651-20659651-0206-23

All 44 Nitrofurantoin NDCs

Other NDCs under ANDA 208516

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

FDA NDC Directory listings under ANDA 208516
ProductStrengthForm · routeLabelerProduct NDC
NitrofurantoinNitrofurantoin 25 mg/1; Nitrofurantoin monohydrate 75 mg/1CapsuleOralTrigen Laboratories, LLC13811-719
NitrofurantoinNitrofurantoin 25 mg/1; Nitrofurantoin monohydrate 75 mg/1CapsuleOralSt. Mary's Medical Park Pharmacy60760-853
NitrofurantoinNitrofurantoin 25 mg/1; Nitrofurantoin monohydrate 75 mg/1CapsuleOralBryant Ranch Prepack63629-2464
NitrofurantoinNitrofurantoin 25 mg/1; Nitrofurantoin monohydrate 75 mg/1CapsuleOralRedpharm Drug, Inc.67296-1442
NitrofurantoinNitrofurantoin 25 mg/1; Nitrofurantoin monohydrate 75 mg/1CapsuleOralNuCare Pharmaceuticals,Inc.68071-2928
NitrofurantoinNitrofurantoin 25 mg/1; Nitrofurantoin monohydrate 75 mg/1CapsuleOralPreferred Pharmaceuticals Inc.68788-8258
NitrofurantoinNitrofurantoin 25 mg/1; Nitrofurantoin monohydrate 75 mg/1CapsuleOralREMEDYREPACK INC.70518-3717
NitrofurantoinNitrofurantoin 25 mg/1; Nitrofurantoin monohydrate 75 mg/1CapsuleOralProficient Rx LP71205-852
NitrofurantoinNitrofurantoin 25 mg/1; Nitrofurantoin monohydrate 75 mg/1CapsuleOralBryant Ranch Prepack71335-2320
NitrofurantoinNitrofurantoin 25 mg/1; Nitrofurantoin monohydrate 75 mg/1CapsuleOralBryant Ranch Prepack71335-2914
NitrofurantoinNitrofurantoin 25 mg/1; Nitrofurantoin monohydrate 75 mg/1CapsuleOralBryant Ranch Prepack72162-1262
NitrofurantoinNitrofurantoin 25 mg/1; Nitrofurantoin monohydrate 75 mg/1CapsuleOralPD-Rx Pharmaceuticals, Inc.72789-386
NitrofurantoinNitrofurantoin 25 mg/1; Nitrofurantoin monohydrate 75 mg/1CapsuleOralPD-Rx Pharmaceuticals, Inc.72789-387
Nitrofurantoin Monohydrate/MacrocrystalNitrofurantoin monohydrate 75 mg/1; Nitrofurantoin 25 mg/1CapsuleOralDirect_Rx72189-395

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