What is NDC 71335-2190?

71335-2190 is the product NDC for Famotidine, Famotidine 20 mg/1 tablet, film coated, 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 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 71335-2190 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-2190Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-2190Add 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
71335-2190-1	7133521900171335219001	30 TABLET, FILM COATED in 1 BOTTLE (71335-2190-1)Marketed from Nov 15, 2022
71335-2190-2	7133521900271335219002	60 TABLET, FILM COATED in 1 BOTTLE (71335-2190-2)Marketed from Nov 15, 2022
71335-2190-3	7133521900371335219003	20 TABLET, FILM COATED in 1 BOTTLE (71335-2190-3)Marketed from Nov 15, 2022
71335-2190-4	7133521900471335219004	90 TABLET, FILM COATED in 1 BOTTLE (71335-2190-4)Marketed from Nov 15, 2022
71335-2190-5	7133521900571335219005	100 TABLET, FILM COATED in 1 BOTTLE (71335-2190-5)Marketed from Nov 15, 2022
71335-2190-6	7133521900671335219006	10 TABLET, FILM COATED in 1 BOTTLE (71335-2190-6)Marketed from Nov 15, 2022
71335-2190-7	7133521900771335219007	120 TABLET, FILM COATED in 1 BOTTLE (71335-2190-7)Marketed from Nov 15, 2022
71335-2190-8	7133521900871335219008	50 TABLET, FILM COATED in 1 BOTTLE (71335-2190-8)Marketed from Nov 15, 2022
71335-2190-9	7133521900971335219009	14 TABLET, FILM COATED in 1 BOTTLE (71335-2190-9)Marketed from Nov 15, 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): 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 216441
Marketing start: Jun 6, 2022
Listing expires: Dec 31, 2026
Other FDA classes: Histamine H2 Receptor Antagonists (Mechanism)
Identifiers: Product ID 71335-2190_ca5b10e6-83a5-475c-8a04-9621381afcfcSPL ID ca5b10e6-83a5-475c-8a04-9621381afcfcSPL set ID 72a97532-9a79-4cbf-b9d0-22ce1f21468dRxCUI 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

N471335219001 followed by a unit qualifier and the quantity

Package 71335-2190-01. 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 Aug 23, 2024.

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. sympto…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-2190

What is NDC 71335-2190?: 71335-2190 is the product NDC for Famotidine, Famotidine 20 mg/1 tablet, film coated, 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?: 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 216441

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

FDA NDC Directory listings under ANDA 216441
Product	Strength	Form · route	Labeler	Product NDC
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Safecor Health, LLC	48433-150
Famotidine	Famotidine 40 mg/1	Tablet, Film coatedOral	St. Mary's Medical Park Pharmacy	60760-736
Famotidine	Famotidine 40 mg/1	Tablet, Film coatedOral	NuCare Pharmaceuticals,Inc.	68071-3521
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Zydus Pharmaceuticals USA Inc.	70710-1683
Famotidine	Famotidine 40 mg/1	Tablet, Film coatedOral	Zydus Pharmaceuticals USA Inc.	70710-1684
Famotidine	Famotidine 20 mg/1	Tablet, Film coatedOral	Zydus Lifesciences Limited	70771-1702
Famotidine	Famotidine 40 mg/1	Tablet, Film coatedOral	Zydus Lifesciences Limited	70771-1703
Famotidine	Famotidine 40 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-9615