Home NDC 72288-151 basic care heartburn prevention
Product NDC 72288-151
11-digit product format 722880151
Labeler code 72288
Product ID 72288-151_1a96c8a0-8899-41e4-8038-dac06cbf5a10
Type HUMAN OTC DRUG
Nonproprietary name famotidine
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Amazon.com Services LLC
Application ANDA077351
Marketing category ANDA
Marketing start 2022-01-05
Substance FAMOTIDINE
Active strength 20 mg/1
Pharmacologic classes Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Source provenance: Browse the complete Orange Book source catalog · source snapshot 1 .
Orange Book products# Current product rows page 1 of 1 · 1 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A077351-001 FAMOTIDINE FAMOTIDINE 20MG TABLET / ORAL 2006-09-25
Observed Orange Book product history# Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
Captured, Edition, Application-product table Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2026-08-01 22:54:32 2026-06 A077351-001 FAMOTIDINE 20MG TABLET / ORAL 2006-09-25 a50c72e98297…
openFDA label cross-check# Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.
Matched openFDA labels page 1 of 3 · 42 matching rows.
Additional Listing Data#
Finished product Yes
Brand name base basic care heartburn prevention
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength FAMOTIDINE 20 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5QZO15J2Z8 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 310273 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72288-151-75 basic care heartburn prevention 1 in 1 CARTON TABLET, FILM COATED 1 3 72288-151-75 basic care heartburn prevention 90 in 1 BOTTLE TABLET, FILM COATED 90 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72288-151 BASIC CARE HEARTBURN PREVENTION (FAMOTIDINE) TABLET, FILM COATED [AMAZON.COM SERVICES LLC] 2 Current NDC, Legacy NDC, 2 package rows 20220121_8d57f6db-a9f0-4416-9f49-17ce3571b0aa.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 72288-151-75 72288015175 1 BOTTLE in 1 CARTON (72288-151-75) / 90 TABLET, FILM COATED in 1 BOTTLE 1 bottle 2022-01-05 0000-00-00 No No Current