Package 71821-012-08

Brand: famotidine

Generic: famotidine
NDC Package

Package Facts

Identity

Package NDC 71821-012-08
Digits Only 7182101208
Product NDC 71821-012
Description

288461 TABLET, FILM COATED in 1 BAG (71821-012-08)

Marketing

Marketing Status
Marketed Since 2022-09-07
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": "0fc43ab9-0e23-258f-e063-6394a90a0c40", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["199047", "310273"], "spl_set_id": ["4e5db906-992f-476b-9d97-63a4c582bbdc"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["VKT Pharma Private Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "288461 TABLET, FILM COATED in 1 BAG (71821-012-08)", "package_ndc": "71821-012-08", "marketing_start_date": "20220907"}], "brand_name": "Famotidine", "product_id": "71821-012_0fc43ab9-0e23-258f-e063-6394a90a0c40", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "71821-012", "generic_name": "Famotidine", "labeler_name": "VKT Pharma Private Limited", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "10 mg/1"}], "application_number": "ANDA215822", "marketing_category": "ANDA", "marketing_start_date": "20220128", "listing_expiration_date": "20261231"}