Package 0378-0317-01

Brand: cimetidine

Generic: cimetidine
NDC Package

Package Facts

Identity

Package NDC 0378-0317-01
Digits Only 0378031701
Product NDC 0378-0317
Description

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0317-01)

Marketing

Marketing Status
Marketed Since 1994-05-17
Brand cimetidine
Generic cimetidine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "14717870-5f24-4002-ada5-1c5a44cc2be9", "openfda": {"nui": ["N0000000151", "N0000175784"], "upc": ["0303780541016", "0303780317017", "0303780053014", "0303780372016"], "unii": ["80061L1WGD"], "rxcui": ["197505", "197506", "197507", "197508"], "spl_set_id": ["06c0a509-026f-44e0-9975-a94a8de51d43"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0317-01)", "package_ndc": "0378-0317-01", "marketing_start_date": "19940517"}], "brand_name": "Cimetidine", "product_id": "0378-0317_14717870-5f24-4002-ada5-1c5a44cc2be9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "0378-0317", "generic_name": "cimetidine", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cimetidine", "active_ingredients": [{"name": "CIMETIDINE", "strength": "300 mg/1"}], "application_number": "ANDA074246", "marketing_category": "ANDA", "marketing_start_date": "19940517", "listing_expiration_date": "20261231"}