famotidine

Generic: famotidine

Labeler: lifestar pharma llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name famotidine
Generic Name famotidine
Labeler lifestar pharma llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

famotidine 40 mg/1

Manufacturer
Lifestar Pharma LLC

Identifiers & Regulatory

Product NDC 70756-052
Product ID 70756-052_8c901736-6453-4cbd-824d-073bc083e6aa
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075302
Listing Expiration 2026-12-31
Marketing Start 2023-10-19

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 70756052
Hyphenated Format 70756-052

Supplemental Identifiers

RxCUI
284245 310273
UPC
0370756051114 0370756052111
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 ANDA075302 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (70756-052-11)
  • 1000 TABLET in 1 BOTTLE (70756-052-12)
source: ndc

Packages (2)

70756-052-11 100 TABLET in 1 BOTTLE (70756-052-11) 70756-052-12 1000 TABLET in 1 BOTTLE (70756-052-12)

Ingredients (1)

famotidine (40 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": "8c901736-6453-4cbd-824d-073bc083e6aa", "openfda": {"nui": ["N0000000151", "N0000175784"], "upc": ["0370756051114", "0370756052111"], "unii": ["5QZO15J2Z8"], "rxcui": ["284245", "310273"], "spl_set_id": ["044a510f-33df-4484-8f07-d821f52b9376"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Lifestar Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70756-052-11)", "package_ndc": "70756-052-11", "marketing_start_date": "20231019"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (70756-052-12)", "package_ndc": "70756-052-12", "marketing_start_date": "20231019"}], "brand_name": "Famotidine", "product_id": "70756-052_8c901736-6453-4cbd-824d-073bc083e6aa", "dosage_form": "TABLET", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "70756-052", "generic_name": "Famotidine", "labeler_name": "Lifestar Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "40 mg/1"}], "application_number": "ANDA075302", "marketing_category": "ANDA", "marketing_start_date": "20231019", "listing_expiration_date": "20261231"}