What is NDC 71335-2805?

71335-2805 is the product NDC for Famotidine, Famotidine 20 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. It has 10 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 71335-2805 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-2805Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-2805Add 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
71335-2805-0	7133528050071335280500	40 TABLET, FILM COATED in 1 BOTTLE (71335-2805-0)Marketed from Oct 14, 2025
71335-2805-1	7133528050171335280501	30 TABLET, FILM COATED in 1 BOTTLE (71335-2805-1)Marketed from Oct 14, 2025
71335-2805-2	7133528050271335280502	60 TABLET, FILM COATED in 1 BOTTLE (71335-2805-2)Marketed from Oct 14, 2025
71335-2805-3	7133528050371335280503	20 TABLET, FILM COATED in 1 BOTTLE (71335-2805-3)Marketed from Oct 14, 2025
71335-2805-4	7133528050471335280504	90 TABLET, FILM COATED in 1 BOTTLE (71335-2805-4)Marketed from Oct 14, 2025
71335-2805-5	7133528050571335280505	100 TABLET, FILM COATED in 1 BOTTLE (71335-2805-5)Marketed from Oct 14, 2025
71335-2805-6	7133528050671335280506	10 TABLET, FILM COATED in 1 BOTTLE (71335-2805-6)Marketed from Oct 14, 2025
71335-2805-7	7133528050771335280507	120 TABLET, FILM COATED in 1 BOTTLE (71335-2805-7)Marketed from Oct 14, 2025
71335-2805-8	7133528050871335280508	50 TABLET, FILM COATED in 1 BOTTLE (71335-2805-8)Marketed from Oct 14, 2025
71335-2805-9	7133528050971335280509	14 TABLET, FILM COATED in 1 BOTTLE (71335-2805-9)Marketed from Oct 14, 2025

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 217400
Marketing start: Aug 6, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Histamine H2 Receptor Antagonists (Mechanism)
Identifiers: Product ID 71335-2805_b2d70cef-4104-46d3-af20-aec60436b34bSPL ID b2d70cef-4104-46d3-af20-aec60436b34bSPL set ID c133a9e1-ca48-4ee2-8768-01f44f5dd511RxCUI 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

N471335280500 followed by a unit qualifier and the quantity

Package 71335-2805-00. 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 Oct 14, 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 gastr…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-2805

What is NDC 71335-2805?: 71335-2805 is the product NDC for Famotidine, Famotidine 20 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. It has 10 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 217400

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

FDA NDC Directory listings under ANDA 217400
Product	Strength	Form · route	Labeler	Product NDC
Famotidine	Famotidine 40 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4394
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4395
Famotidine	Famotidine 40 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-4144
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Advanced Rx of Tennessee, LLC	80425-0589
Famotidine	Famotidine 40 mg/1	Tablet, Film coatedOral	Novadoz Pharmaceuticals LLC	72205-146
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Novadoz Pharmaceuticals LLC	72205-145
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-4021
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Redpharm Drug	67296-2186