famotidine

Generic: famotidine

Labeler: carlsbad technology, inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name famotidine
Generic Name famotidine
Labeler carlsbad technology, inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

famotidine 20 mg/1

Manufacturer
Carlsbad Technology, Inc

Identifiers & Regulatory

Product NDC 61442-121
Product ID 61442-121_206161c2-b8ce-04c1-e063-6294a90ac404
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075805
Listing Expiration 2026-12-31
Marketing Start 2001-04-16

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 61442121
Hyphenated Format 61442-121

Supplemental Identifiers

RxCUI
284245 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 famotidine (source: ndc)
Generic Name famotidine (source: ndc)
Application Number ANDA075805 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 24 BOTTLE in 1 BOX (61442-121-01) / 100 TABLET in 1 BOTTLE
  • 24 BOTTLE in 1 BOX (61442-121-05) / 500 TABLET in 1 BOTTLE
  • 12 BOTTLE in 1 BOX (61442-121-10) / 1000 TABLET in 1 BOTTLE
  • 24 BOTTLE in 1 BOX (61442-121-30) / 30 TABLET in 1 BOTTLE
source: ndc

Packages (4)

61442-121-01 24 BOTTLE in 1 BOX (61442-121-01) / 100 TABLET in 1 BOTTLE 61442-121-05 24 BOTTLE in 1 BOX (61442-121-05) / 500 TABLET in 1 BOTTLE 61442-121-10 12 BOTTLE in 1 BOX (61442-121-10) / 1000 TABLET in 1 BOTTLE 61442-121-30 24 BOTTLE in 1 BOX (61442-121-30) / 30 TABLET in 1 BOTTLE

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": "206161c2-b8ce-04c1-e063-6294a90ac404", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["284245", "310273"], "spl_set_id": ["a8b5c855-053d-4295-8f57-1a96a6ccaa92"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Carlsbad Technology, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 BOTTLE in 1 BOX (61442-121-01)  / 100 TABLET in 1 BOTTLE", "package_ndc": "61442-121-01", "marketing_start_date": "20010416"}, {"sample": false, "description": "24 BOTTLE in 1 BOX (61442-121-05)  / 500 TABLET in 1 BOTTLE", "package_ndc": "61442-121-05", "marketing_start_date": "20010416"}, {"sample": false, "description": "12 BOTTLE in 1 BOX (61442-121-10)  / 1000 TABLET in 1 BOTTLE", "package_ndc": "61442-121-10", "marketing_start_date": "20010416"}, {"sample": false, "description": "24 BOTTLE in 1 BOX (61442-121-30)  / 30 TABLET in 1 BOTTLE", "package_ndc": "61442-121-30", "marketing_start_date": "20010416"}], "brand_name": "Famotidine", "product_id": "61442-121_206161c2-b8ce-04c1-e063-6294a90ac404", "dosage_form": "TABLET", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "61442-121", "generic_name": "Famotidine", "labeler_name": "Carlsbad Technology, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "20 mg/1"}], "application_number": "ANDA075805", "marketing_category": "ANDA", "marketing_start_date": "20010416", "listing_expiration_date": "20261231"}