Package 67296-2133-3

Brand: famotidine

Generic: famotidine
NDC Package

Package Facts

Identity

Package NDC 67296-2133-3
Digits Only 6729621333
Product NDC 67296-2133
Description

30 TABLET in 1 BOTTLE (67296-2133-3)

Marketing

Marketing Status
Marketed Since 2023-10-19
Brand famotidine
Generic famotidine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "46aca2aa-0c5d-7520-e063-6394a90a959f", "openfda": {"nui": ["N0000000151", "N0000175784"], "upc": ["0370756051114", "0370756052111"], "unii": ["5QZO15J2Z8"], "rxcui": ["310273"], "spl_set_id": ["37361ccf-e080-d58e-e063-6394a90ab92e"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (67296-2133-3)", "package_ndc": "67296-2133-3", "marketing_start_date": "20231019"}], "brand_name": "Famotidine", "product_id": "67296-2133_46aca2aa-0c5d-7520-e063-6394a90a959f", "dosage_form": "TABLET", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "67296-2133", "generic_name": "Famotidine", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "20 mg/1"}], "application_number": "ANDA075302", "marketing_category": "ANDA", "marketing_start_date": "20231019", "listing_expiration_date": "20261231"}