What is NDC 71335-0024?

71335-0024 is the product NDC for Nitrofurantion, Nitrofurantoin 100 mg/1 capsule, listed with the FDA by Bryant Ranch Prepack. It has 9 package NDCs, shown above in 10- and 11-digit form.

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 Nitrofurantion?

9 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Nitrofurantion NDC 71335-0024 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-0024Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-0024Add 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 NDC	11-digit (billing)	Package
71335-0024-1	7133500240171335002401	40 CAPSULE in 1 BOTTLE (71335-0024-1)Marketed from Feb 22, 2022
71335-0024-2	7133500240271335002402	28 CAPSULE in 1 BOTTLE (71335-0024-2)Marketed from Mar 17, 2020
71335-0024-3	7133500240371335002403	30 CAPSULE in 1 BOTTLE (71335-0024-3)Marketed from Feb 22, 2022
71335-0024-4	7133500240471335002404	20 CAPSULE in 1 BOTTLE (71335-0024-4)Marketed from Mar 9, 2020
71335-0024-5	7133500240571335002405	14 CAPSULE in 1 BOTTLE (71335-0024-5)Marketed from Dec 30, 2019
71335-0024-6	7133500240671335002406	10 CAPSULE in 1 BOTTLE (71335-0024-6)Marketed from Dec 23, 2019
71335-0024-7	7133500240771335002407	12 CAPSULE in 1 BOTTLE (71335-0024-7)Marketed from Feb 22, 2022
71335-0024-8	7133500240871335002408	90 CAPSULE in 1 BOTTLE (71335-0024-8)Marketed from Feb 22, 2022
71335-0024-9	7133500240971335002409	6 CAPSULE in 1 BOTTLE (71335-0024-9)Marketed from Feb 22, 2022

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): Nitrofurantion
Generic name (nonproprietary): nitrofurantion
Active ingredients: Nitrofurantoin — 100 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 201722
Marketing start: Apr 15, 2016
Listing expires: Dec 31, 2027
Other FDA classes: Nitrofurans (Chemical structure)
Identifiers: Product ID 71335-0024_ab055bc5-fe67-400c-acf2-49283109c765SPL ID ab055bc5-fe67-400c-acf2-49283109c765SPL set ID eeb12928-61ab-42a0-a1fa-2819b9ffa3cbRxCUI 1648759UNII 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

N471335002401 followed by a unit qualifier and the quantity

Package 71335-0024-01. 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 Jun 24, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE: Nitrofurantoin Capsules, USP (macrocrystals) 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 Nitrofurantoin Capsules, USP (macrocrystals) and other antibacterial drugs, Nitrofurantoin Capsules, USP (macrocrystals) should be used only to treat or prevent infections that are proven or strongly suspected to be ca…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-0024

What is NDC 71335-0024?: 71335-0024 is the product NDC for Nitrofurantion, Nitrofurantoin 100 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?: Nitrofurantion.
What is the active ingredient?: Nitrofurantoin.
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 Nitrofurantion?: 9 other product NDCs are listed under this name. See all Nitrofurantion 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 Nitrofurantion NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Nitrofurantion	Nitrofurantoin 25 mg/1	CapsuleOral	BluePoint Labortories	68001-384	68001-0384-00
Nitrofurantion	Nitrofurantoin 50 mg/1	CapsuleOral	BluePoint Labortories	68001-385	68001-0385-00
Nitrofurantion	Nitrofurantoin 100 mg/1	CapsuleOral	BluePoint Labortories	68001-386	68001-0386-00
Nitrofurantion	Nitrofurantoin 100 mg/1	CapsuleOral	A-S Medication Solutions	50090-5693	50090-5693-0050090-5693-0250090-5693-03
Nitrofurantion	Nitrofurantoin 25 mg/1	CapsuleOral	Sun Pharmaceutical Industries, Inc.	57664-231	57664-0231-1857664-0231-88
Nitrofurantion	Nitrofurantoin 50 mg/1	CapsuleOral	Sun Pharmaceutical Industries, Inc.	57664-232	57664-0232-1857664-0232-88
Nitrofurantion	Nitrofurantoin 100 mg/1	CapsuleOral	Sun Pharmaceutical Industries, Inc.	57664-233	57664-0233-1857664-0233-88
Nitrofurantion	Nitrofurantoin 100 mg/1	CapsuleOral	NuCare Pharmaceuticals,Inc.	68071-2363	68071-2363-0768071-2363-08
Nitrofurantion	Nitrofurantoin 100 mg/1	CapsuleOral	Proficient Rx LP	71205-171	71205-0171-1071205-0171-1471205-0171-20+1 more

Other NDCs under ANDA 201722

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

FDA NDC Directory listings under ANDA 201722
Product	Strength	Form · route	Labeler	Product NDC
Nitrofurantion	Nitrofurantoin 100 mg/1	CapsuleOral	A-S Medication Solutions	50090-5693
Nitrofurantion	Nitrofurantoin 25 mg/1	CapsuleOral	Sun Pharmaceutical Industries, Inc.	57664-231
Nitrofurantion	Nitrofurantoin 50 mg/1	CapsuleOral	Sun Pharmaceutical Industries, Inc.	57664-232
Nitrofurantion	Nitrofurantoin 100 mg/1	CapsuleOral	Sun Pharmaceutical Industries, Inc.	57664-233
Nitrofurantion	Nitrofurantoin 25 mg/1	CapsuleOral	BluePoint Labortories	68001-384
Nitrofurantion	Nitrofurantoin 50 mg/1	CapsuleOral	BluePoint Labortories	68001-385
Nitrofurantion	Nitrofurantoin 100 mg/1	CapsuleOral	BluePoint Labortories	68001-386
Nitrofurantion	Nitrofurantoin 100 mg/1	CapsuleOral	NuCare Pharmaceuticals,Inc.	68071-2363
Nitrofurantion	Nitrofurantoin 100 mg/1	CapsuleOral	Proficient Rx LP	71205-171