What is NDC 71335-0370?

71335-0370 is the product NDC for Famotidine, Famotidine 20 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. It has 8 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 Famotidine?

252 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Famotidine NDC 71335-0370 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-0370Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-0370Add 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
71335-0370-1	7133503700171335037001	30 TABLET, FILM COATED in 1 BOTTLE (71335-0370-1)Marketed from Apr 16, 2021
71335-0370-2	7133503700271335037002	60 TABLET, FILM COATED in 1 BOTTLE (71335-0370-2)Marketed from Jul 23, 2021
71335-0370-3	7133503700371335037003	20 TABLET, FILM COATED in 1 BOTTLE (71335-0370-3)Marketed from Dec 27, 2021
71335-0370-4	7133503700471335037004	90 TABLET, FILM COATED in 1 BOTTLE (71335-0370-4)Marketed from May 4, 2021
71335-0370-5	7133503700571335037005	100 TABLET, FILM COATED in 1 BOTTLE (71335-0370-5)Marketed from Dec 27, 2021
71335-0370-6	7133503700671335037006	10 TABLET, FILM COATED in 1 BOTTLE (71335-0370-6)Marketed from Jun 29, 2021
71335-0370-7	7133503700771335037007	120 TABLET, FILM COATED in 1 BOTTLE (71335-0370-7)Marketed from Sep 2, 2021
71335-0370-8	7133503700871335037008	50 TABLET, FILM COATED in 1 BOTTLE (71335-0370-8)Marketed from Dec 27, 2021

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): Famotidine
Generic name (nonproprietary): famotidine
Active ingredients: Famotidine — 20 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 71335
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 206530
Marketing start: Dec 22, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Histamine H2 Receptor Antagonists (Mechanism)
Identifiers: Product ID 71335-0370_337a85de-6910-03aa-e063-6294a90a2e71SPL ID 337a85de-6910-03aa-e063-6294a90a2e71SPL set ID 11ce2a78-76ce-44df-afe3-57493498e596RxCUI 310273UNII 5QZO15J2Z8
Pharmacologic class: Histamine-2 Receptor Antagonist

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

N471335037001 followed by a unit qualifier and the quantity

Package 71335-0370-01. 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 Apr 23, 2025.

Indications (excerpt from the label)

Famotidine tablets are indicated in adult and pediatric patients 40 kg and greater for the treatment of: active duodenal ulcer (DU). active gastric ulcer (GU). symptomatic nonerosive gastroesophageal reflux disease (GERD). erosive esophagitis due to GERD, diagnosed by biopsy. Famotidine tablets are indicated in adults for the: treatment of pathological hypersecretory conditions (e.g., Zollinger-Ellison syndrome, multiple endocrine neoplasias). reduction of the risk of duodenal ulcer recurrence. Famotidine is a histamine-2 (H 2 ) receptor antagonist indicated (1) : In adult and pediatric patients 40 kg and greater for the treatment of: active duodenal ulcer (DU). active gastric ulcer. symptom…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-0370

What is NDC 71335-0370?: 71335-0370 is the product NDC for Famotidine, Famotidine 20 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. It has 8 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Famotidine.
What is the active ingredient?: Famotidine.
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 Famotidine?: 252 other product NDCs are listed under this name. See all Famotidine 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 Famotidine NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Famotidine	Famotidine 40 mg/5mL	Powder, For suspensionOral	NorthStar Rx LLC	72603-564	72603-0564-01
Famotidine	Famotidine 40 mg/5mL	Powder, For suspensionOral	RISING PHARMA HOLDINGS, INC.	64980-737	64980-0737-50
Famotidine	Famotidine 40 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-4144	68788-4144-0368788-4144-0468788-4144-06+1 more
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Advanced Rx of Tennessee, LLC	80425-0589	80425-0589-0180425-0589-0280425-0589-03
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Family Dollar Stores, LLC	55319-057	55319-0057-1055319-0057-2555319-0057-50
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Unit Dose Solutions, Inc.	87441-030	87441-0030-01
Famotidine	Famotidine 20 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4119	68788-4119-0168788-4119-0368788-4119-04+3 more
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Safecor Health, LLC	48433-150	48433-0150-20
Famotidine	Famotidine 20 mg/1	Tablet, CoatedOral	Preferred Pharmaceuticals Inc.	68788-4088	68788-4088-0368788-4088-0468788-4088-06+1 more
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4574	70518-4574-0070518-4574-0170518-4574-02+1 more

All 253 Famotidine NDCs

Other NDCs under ANDA 206530

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

FDA NDC Directory listings under ANDA 206530
Product	Strength	Form · route	Labeler	Product NDC
Famotidine	Famotidine 40 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-6916
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	American Health Packaging	60687-595
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	BluePoint Laboratories	68001-397
Famotidine	Famotidine 40 mg/1	Tablet, Film coatedOral	BluePoint Laboratories	68001-398
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Proficient Rx LP	71205-535
Famotidine	Famotidine 40 mg/1	Tablet, Film coatedOral	Proficient Rx LP	71205-634
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Unit Dose Solutions, Inc.	87441-030