maximum strength

Generic: famotidine

Labeler: publix super markets inc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name maximum strength
Generic Name famotidine
Labeler publix super markets inc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

famotidine 20 mg/1

Manufacturer
Publix Super Markets Inc

Identifiers & Regulatory

Product NDC 56062-194
Product ID 56062-194_106cff2c-1d3b-4f5d-ab79-5f67e04594d6
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA077351
Listing Expiration 2026-12-31
Marketing Start 2007-12-03

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 56062194
Hyphenated Format 56062-194

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 maximum strength (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
  • 25 BLISTER PACK in 1 CARTON (56062-194-02) / 1 TABLET, FILM COATED in 1 BLISTER PACK
  • 1 BOTTLE in 1 CARTON (56062-194-71) / 50 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (2)

56062-194-02 25 BLISTER PACK in 1 CARTON (56062-194-02) / 1 TABLET, FILM COATED in 1 BLISTER PACK 56062-194-71 1 BOTTLE in 1 CARTON (56062-194-71) / 50 TABLET, FILM COATED in 1 BOTTLE

Ingredients (1)

famotidine (20 mg/1)

Linked Drug Pages (1)

maximum strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "106cff2c-1d3b-4f5d-ab79-5f67e04594d6", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["310273"], "spl_set_id": ["f692ed61-d09a-484e-bf07-8afcedfb3208"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Publix Super Markets Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 BLISTER PACK in 1 CARTON (56062-194-02)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "56062-194-02", "marketing_start_date": "20071203"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (56062-194-71)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "56062-194-71", "marketing_start_date": "20071207"}], "brand_name": "maximum strength", "product_id": "56062-194_106cff2c-1d3b-4f5d-ab79-5f67e04594d6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "56062-194", "generic_name": "Famotidine", "labeler_name": "Publix Super Markets Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "maximum strength", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "20 mg/1"}], "application_number": "ANDA077351", "marketing_category": "ANDA", "marketing_start_date": "20071203", "listing_expiration_date": "20261231"}