famotidine

Generic: famotidine

Labeler: alembic pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name famotidine
Generic Name famotidine
Labeler alembic pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

famotidine 20 mg/1

Manufacturer
Alembic Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 62332-001
Product ID 62332-001_bd221da3-ca77-4407-856b-489a8903c842
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078916
Listing Expiration 2027-12-31
Marketing Start 2016-01-29

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 62332001
Hyphenated Format 62332-001

Supplemental Identifiers

RxCUI
284245 310273
UPC
0362332002306 0362332001309
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 famotidine (source: ndc)
Generic Name famotidine (source: ndc)
Application Number ANDA078916 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 CARTON (62332-001-10)
  • 30 TABLET in 1 BOTTLE (62332-001-30)
  • 100 TABLET in 1 BOTTLE (62332-001-31)
  • 500 TABLET in 1 BOTTLE (62332-001-71)
  • 1000 TABLET in 1 BOTTLE (62332-001-91)
source: ndc

Packages (5)

62332-001-10 100 TABLET in 1 CARTON (62332-001-10) 62332-001-30 30 TABLET in 1 BOTTLE (62332-001-30) 62332-001-31 100 TABLET in 1 BOTTLE (62332-001-31) 62332-001-71 500 TABLET in 1 BOTTLE (62332-001-71) 62332-001-91 1000 TABLET in 1 BOTTLE (62332-001-91)

Ingredients (1)

famotidine (20 mg/1)

Linked Drug Pages (1)

Famotidine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "bd221da3-ca77-4407-856b-489a8903c842", "openfda": {"nui": ["N0000000151", "N0000175784"], "upc": ["0362332002306", "0362332001309"], "unii": ["5QZO15J2Z8"], "rxcui": ["284245", "310273"], "spl_set_id": ["f149ecc1-d66c-42f9-a3f4-2ab6a522942b"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 CARTON (62332-001-10)", "package_ndc": "62332-001-10", "marketing_start_date": "20160129"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (62332-001-30)", "package_ndc": "62332-001-30", "marketing_start_date": "20160129"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (62332-001-31)", "package_ndc": "62332-001-31", "marketing_start_date": "20160129"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (62332-001-71)", "package_ndc": "62332-001-71", "marketing_start_date": "20160129"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (62332-001-91)", "package_ndc": "62332-001-91", "marketing_start_date": "20160129"}], "brand_name": "Famotidine", "product_id": "62332-001_bd221da3-ca77-4407-856b-489a8903c842", "dosage_form": "TABLET", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "62332-001", "generic_name": "Famotidine", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "20 mg/1"}], "application_number": "ANDA078916", "marketing_category": "ANDA", "marketing_start_date": "20160129", "listing_expiration_date": "20271231"}