famotidine
Generic: famotidine
Labeler: family dollarDrug Facts
Product Profile
Brand Name
famotidine
Generic Name
famotidine
Labeler
family dollar
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
famotidine 20 mg/1
Manufacturer
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)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55319409
Hyphenated Format
55319-409
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 20 mg/1
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
Packages (3)
Ingredients (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"}