famotidine
Generic: famotidine
Labeler: cvs pharmacy, inc.Drug Facts
Product Profile
Brand Name
famotidine
Generic Name
famotidine
Labeler
cvs pharmacy, inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
famotidine 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
69842-063
Product ID
69842-063_b2736a1a-a748-45a8-8a9b-289f7dd61d14
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA206531
Listing Expiration
2026-12-31
Marketing Start
2020-02-03
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69842063
Hyphenated Format
69842-063
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
ANDA206531 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (69842-063-19) / 90 TABLET, FILM COATED in 1 BOTTLE
- 2 BOTTLE in 1 CARTON (69842-063-79) / 90 TABLET, FILM COATED in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (69842-063-84) / 30 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": "b2736a1a-a748-45a8-8a9b-289f7dd61d14", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["199047"], "spl_set_id": ["7357f67e-0fc6-4555-aa8b-1df09cba9feb"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["CVS Pharmacy, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (69842-063-19) / 90 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "69842-063-19", "marketing_start_date": "20200203"}, {"sample": false, "description": "2 BOTTLE in 1 CARTON (69842-063-79) / 90 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "69842-063-79", "marketing_start_date": "20210125"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (69842-063-84) / 30 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "69842-063-84", "marketing_start_date": "20200203"}], "brand_name": "Famotidine", "product_id": "69842-063_b2736a1a-a748-45a8-8a9b-289f7dd61d14", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "69842-063", "generic_name": "Famotidine", "labeler_name": "CVS Pharmacy, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "10 mg/1"}], "application_number": "ANDA206531", "marketing_category": "ANDA", "marketing_start_date": "20200203", "listing_expiration_date": "20261231"}