acid reducer

Generic: famotidine

Labeler: h e b
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acid reducer
Generic Name famotidine
Labeler h e b
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

famotidine 20 mg/1

Manufacturer
H E B

Identifiers & Regulatory

Product NDC 59640-023
Product ID 59640-023_b8b7bb2e-3c48-4aba-a4cb-b33b70383fd0
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA077351
Listing Expiration 2027-12-31
Marketing Start 2022-12-19

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 59640023
Hyphenated Format 59640-023

Supplemental Identifiers

RxCUI
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 acid reducer (source: ndc)
Generic Name famotidine (source: ndc)
Application Number ANDA077351 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (59640-023-71) / 50 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (1)

59640-023-71 1 BOTTLE in 1 CARTON (59640-023-71) / 50 TABLET, FILM COATED in 1 BOTTLE

Ingredients (1)

famotidine (20 mg/1)

Linked Drug Pages (1)

acid reducer ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b8b7bb2e-3c48-4aba-a4cb-b33b70383fd0", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["310273"], "spl_set_id": ["140f0e60-c809-4d86-a750-7649ee2881b5"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (59640-023-71)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "59640-023-71", "marketing_start_date": "20221219"}], "brand_name": "acid reducer", "product_id": "59640-023_b8b7bb2e-3c48-4aba-a4cb-b33b70383fd0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "59640-023", "generic_name": "famotidine", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "acid reducer", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "20 mg/1"}], "application_number": "ANDA077351", "marketing_category": "ANDA", "marketing_start_date": "20221219", "listing_expiration_date": "20271231"}