famotidine

Generic: famotidine

Labeler: family dollar
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name famotidine
Generic Name famotidine
Labeler family dollar
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

famotidine 20 mg/1

Manufacturer
FAMILY DOLLAR

Identifiers & Regulatory

Product NDC 55319-409
Product ID 55319-409_99698eea-6bf1-42e8-9f48-d58fc0437324
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA215822
Listing Expiration 2026-12-31
Marketing Start 2025-09-01

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 55319409
Hyphenated Format 55319-409

Supplemental Identifiers

RxCUI
199047 310273
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 (source: ndc)
Generic Name famotidine (source: ndc)
Application Number ANDA215822 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (55319-409-01) / 25 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (55319-409-02) / 50 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (55319-409-03) / 100 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (3)

Ingredients (1)

famotidine (20 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "99698eea-6bf1-42e8-9f48-d58fc0437324", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["199047", "310273"], "spl_set_id": ["99698eea-6bf1-42e8-9f48-d58fc0437324"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["FAMILY DOLLAR"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (55319-409-01)  / 25 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "55319-409-01", "marketing_start_date": "20250901"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (55319-409-02)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "55319-409-02", "marketing_start_date": "20250901"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (55319-409-03)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "55319-409-03", "marketing_start_date": "20250901"}], "brand_name": "Famotidine", "product_id": "55319-409_99698eea-6bf1-42e8-9f48-d58fc0437324", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "55319-409", "generic_name": "Famotidine", "labeler_name": "FAMILY DOLLAR", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "20 mg/1"}], "application_number": "ANDA215822", "marketing_category": "ANDA", "marketing_start_date": "20250901", "listing_expiration_date": "20261231"}