famotidine

Generic: famotidine

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

Drug Facts

Product Profile

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

famotidine 40 mg/5mL

Manufacturer
Lupin Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68180-150
Product ID 68180-150_ce0e39ea-0d29-4922-95cb-8777326a994e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090440
Listing Expiration 2026-12-31
Marketing Start 2010-06-29

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 68180150
Hyphenated Format 68180-150

Supplemental Identifiers

RxCUI
310274
UPC
0368180150015
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 ANDA090440 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/5mL
source: ndc
Packaging
  • 50 mL in 1 BOTTLE (68180-150-01)
source: ndc

Packages (1)

68180-150-01 50 mL in 1 BOTTLE (68180-150-01)

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": "ce0e39ea-0d29-4922-95cb-8777326a994e", "openfda": {"nui": ["N0000000151", "N0000175784"], "upc": ["0368180150015"], "unii": ["5QZO15J2Z8"], "rxcui": ["310274"], "spl_set_id": ["2caaf94b-b382-4573-8614-57815776b659"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 BOTTLE (68180-150-01)", "package_ndc": "68180-150-01", "marketing_start_date": "20100629"}], "brand_name": "Famotidine", "product_id": "68180-150_ce0e39ea-0d29-4922-95cb-8777326a994e", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "68180-150", "generic_name": "Famotidine", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "40 mg/5mL"}], "application_number": "ANDA090440", "marketing_category": "ANDA", "marketing_start_date": "20100629", "listing_expiration_date": "20261231"}