Package 71821-012-09

Brand: famotidine

Generic: famotidine
NDC Package

Package Facts

Identity

Package NDC 71821-012-09
Digits Only 7182101209
Product NDC 71821-012
Description

288461 TABLET, FILM COATED in 1 BAG (71821-012-09)

Marketing

Marketing Status
Marketed Since 2024-05-23
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": "6363f098-8bab-4879-bea8-41b60c4530eb", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["199047", "310273"], "spl_set_id": ["1c2cfb3c-eaa0-403f-9589-d706afc06f51"], "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 (71821-012-09)", "package_ndc": "71821-012-09", "marketing_start_date": "20240523"}], "brand_name": "Famotidine", "product_id": "71821-012_6363f098-8bab-4879-bea8-41b60c4530eb", "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": "20240523", "listing_expiration_date": "20261231"}