up and up famotidine

Generic: Famotidine

Labeler: Target Corporation
NDC Directory HUMAN OTC DRUG ANDA Active

Drug Facts

Product Profile

Brand Name up and up famotidine
Generic Name Famotidine
Labeler Target Corporation
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

FAMOTIDINE 20 mg/1

Identifiers & Regulatory

Product NDC 11673-061
Product ID 11673-061_a6f8e898-b673-4cd5-a81d-726d9bdffc05
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA077351
Listing Expiration 2026-12-31
Marketing Start 2012-05-03

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11673061
Hyphenated Format 11673-061

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 up and up famotidine (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 (11673-061-02) / 1 TABLET, FILM COATED in 1 BLISTER PACK
  • 1 BOTTLE in 1 CARTON (11673-061-71) / 50 TABLET, FILM COATED in 1 BOTTLE
  • 2 BOTTLE in 1 CARTON (11673-061-78) / 50 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (11673-061-82) / 200 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (4)

11673-061-02 25 BLISTER PACK in 1 CARTON (11673-061-02) / 1 TABLET, FILM COATED in 1 BLISTER PACK 11673-061-71 1 BOTTLE in 1 CARTON (11673-061-71) / 50 TABLET, FILM COATED in 1 BOTTLE 11673-061-78 2 BOTTLE in 1 CARTON (11673-061-78) / 50 TABLET, FILM COATED in 1 BOTTLE 11673-061-82 1 BOTTLE in 1 CARTON (11673-061-82) / 200 TABLET, FILM COATED in 1 BOTTLE

Ingredients (1)

FAMOTIDINE (20 mg/1)

Linked Drug Pages (1)

up and up famotidine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a6f8e898-b673-4cd5-a81d-726d9bdffc05", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["310273"], "spl_set_id": ["ed8d76c0-3ba2-48b3-ad8b-9f1ea1bd0e41"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 BLISTER PACK in 1 CARTON (11673-061-02)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "11673-061-02", "marketing_start_date": "20120503"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-061-71)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "11673-061-71", "marketing_start_date": "20120514"}, {"sample": false, "description": "2 BOTTLE in 1 CARTON (11673-061-78)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "11673-061-78", "marketing_start_date": "20200417"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-061-82)  / 200 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "11673-061-82", "marketing_start_date": "20211124"}], "brand_name": "up and up famotidine", "product_id": "11673-061_a6f8e898-b673-4cd5-a81d-726d9bdffc05", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "11673-061", "generic_name": "Famotidine", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "up and up famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "20 mg/1"}], "application_number": "ANDA077351", "marketing_category": "ANDA", "marketing_start_date": "20120503", "listing_expiration_date": "20261231"}