famotidine

Generic: famotidine

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

Drug Facts

Product Profile

Brand Name famotidine
Generic Name famotidine
Labeler ani pharmaceuticals, inc.
Dosage Form POWDER, FOR SUSPENSION
Routes
ORAL
Active Ingredients

famotidine 40 mg/5mL

Manufacturer
ANI Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 70954-316
Product ID 70954-316_5dd78321-82a9-48a6-9974-d8d27e9785cf
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215043
Listing Expiration 2026-12-31
Marketing Start 2021-04-20

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 70954316
Hyphenated Format 70954-316

Supplemental Identifiers

RxCUI
310274
UPC
0370954316107
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 ANDA215043 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/5mL
source: ndc
Packaging
  • 50 mL in 1 BOTTLE (70954-316-10)
source: ndc

Packages (1)

70954-316-10 50 mL in 1 BOTTLE (70954-316-10)

Ingredients (1)

famotidine (40 mg/5mL)

Linked Drug Pages (1)

Famotidine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5dd78321-82a9-48a6-9974-d8d27e9785cf", "openfda": {"nui": ["N0000000151", "N0000175784"], "upc": ["0370954316107"], "unii": ["5QZO15J2Z8"], "rxcui": ["310274"], "spl_set_id": ["8e41e259-b161-4f11-a6f7-14e6b60885b8"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 BOTTLE (70954-316-10)", "package_ndc": "70954-316-10", "marketing_start_date": "20210420"}], "brand_name": "Famotidine", "product_id": "70954-316_5dd78321-82a9-48a6-9974-d8d27e9785cf", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "70954-316", "generic_name": "Famotidine", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "40 mg/5mL"}], "application_number": "ANDA215043", "marketing_category": "ANDA", "marketing_start_date": "20210420", "listing_expiration_date": "20261231"}