famotidine 20 mg (25000-124)

Drug Facts

Product Profile

Brand Name famotidine 20 mg

Generic Name famotidine 20 mg

Labeler marksans pharma limited

Dosage Form TABLET, COATED

Routes

ORAL

Active Ingredients

famotidine 20 mg/1

Manufacturer

MARKSANS PHARMA LIMITED

Identifiers & Regulatory

Product NDC 25000-124

Product ID 25000-124_1c69fac1-3052-45b1-ab46-a3b523347de1

Product Type HUMAN OTC DRUG

Marketing Category ANDA

Application Number ANDA217543

Listing Expiration 2026-12-31

Marketing Start 2025-05-23

Pharmacologic Class

Established (EPC)

histamine-2 receptor antagonist [epc]

Mechanism of Action

histamine h2 receptor antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 25000124

Hyphenated Format 25000-124

Supplemental Identifiers

RxCUI

310273

UPC

0325000124847 0325000124687 0325000124946

UNII

5QZO15J2Z8

NUI

N0000000151 N0000175784

Packaging Origin

Original Packager

true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name famotidine 20 mg (source: ndc)

Generic Name famotidine 20 mg (source: ndc)

Application Number ANDA217543 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

20 mg/1

source: ndc

Packaging

300 TABLET, COATED in 1 BOTTLE (25000-124-68)
1 BOTTLE in 1 CARTON (25000-124-84) / 25 TABLET, COATED in 1 BOTTLE
5 BLISTER PACK in 1 CARTON (25000-124-94) / 5 TABLET, COATED in 1 BLISTER PACK

source: ndc

Packages (3)

25000-124-68 300 TABLET, COATED in 1 BOTTLE (25000-124-68) 25000-124-84 1 BOTTLE in 1 CARTON (25000-124-84) / 25 TABLET, COATED in 1 BOTTLE 25000-124-94 5 BLISTER PACK in 1 CARTON (25000-124-94) / 5 TABLET, COATED in 1 BLISTER PACK

Ingredients (1)

famotidine (20 mg/1)

Linked Drug Pages (1)

Famotidine 20 mg ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "1c69fac1-3052-45b1-ab46-a3b523347de1", "openfda": {"nui": ["N0000000151", "N0000175784"], "upc": ["0325000124847", "0325000124687", "0325000124946"], "unii": ["5QZO15J2Z8"], "rxcui": ["310273"], "spl_set_id": ["5a66206b-35b1-4d86-8574-a1e45cb0772f"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["MARKSANS PHARMA LIMITED"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "300 TABLET, COATED in 1 BOTTLE (25000-124-68)", "package_ndc": "25000-124-68", "marketing_start_date": "20250523"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (25000-124-84)  / 25 TABLET, COATED in 1 BOTTLE", "package_ndc": "25000-124-84", "marketing_start_date": "20250523"}, {"sample": false, "description": "5 BLISTER PACK in 1 CARTON (25000-124-94)  / 5 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "25000-124-94", "marketing_start_date": "20250523"}], "brand_name": "Famotidine 20 mg", "product_id": "25000-124_1c69fac1-3052-45b1-ab46-a3b523347de1", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "25000-124", "generic_name": "Famotidine 20 mg", "labeler_name": "MARKSANS PHARMA LIMITED", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Famotidine 20 mg", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "20 mg/1"}], "application_number": "ANDA217543", "marketing_category": "ANDA", "marketing_start_date": "20250523", "listing_expiration_date": "20261231"}