Package 72789-219-08

Brand: nifedipine

Generic: nifedipine
NDC Package

Package Facts

Identity

Package NDC 72789-219-08
Digits Only 7278921908
Product NDC 72789-219
Description

8 CAPSULE in 1 BOTTLE, PLASTIC (72789-219-08)

Marketing

Marketing Status
Marketed Since 2021-12-15
Brand nifedipine
Generic nifedipine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "40ad017c-d405-29e8-e063-6294a90a6edc", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "upc": ["0372789219080"], "unii": ["I9ZF7L6G2L"], "rxcui": ["198032"], "spl_set_id": ["51cdb22b-035f-47d7-8048-38006e2589f2"], "pharm_class_cs": ["Dihydropyridines [CS]"], "pharm_class_epc": ["Dihydropyridine Calcium Channel Blocker [EPC]"], "pharm_class_moa": ["Calcium Channel Antagonists [MoA]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "8 CAPSULE in 1 BOTTLE, PLASTIC (72789-219-08)", "package_ndc": "72789-219-08", "marketing_start_date": "20211215"}], "brand_name": "Nifedipine", "product_id": "72789-219_40ad017c-d405-29e8-e063-6294a90a6edc", "dosage_form": "CAPSULE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "72789-219", "generic_name": "Nifedipine", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nifedipine", "active_ingredients": [{"name": "NIFEDIPINE", "strength": "10 mg/1"}], "application_number": "ANDA202644", "marketing_category": "ANDA", "marketing_start_date": "20101207", "listing_expiration_date": "20261231"}