Package 50268-597-15

Brand: nifedipine er

Generic: nifedipine
NDC Package

Package Facts

Identity

Package NDC 50268-597-15
Digits Only 5026859715
Product NDC 50268-597
Description

50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-597-15) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (50268-597-11)

Marketing

Marketing Status
Marketed Since 2011-02-11
Brand nifedipine er
Generic nifedipine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47e7d21f-e346-6413-e063-6294a90aa9be", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "unii": ["I9ZF7L6G2L"], "rxcui": ["1812011", "1812013", "1812015"], "spl_set_id": ["d1a78ff2-7672-3e69-00ef-63d203c80484"], "pharm_class_cs": ["Dihydropyridines [CS]"], "pharm_class_epc": ["Dihydropyridine Calcium Channel Blocker [EPC]"], "pharm_class_moa": ["Calcium Channel Antagonists [MoA]"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-597-15)  / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (50268-597-11)", "package_ndc": "50268-597-15", "marketing_start_date": "20110211"}], "brand_name": "Nifedipine ER", "product_id": "50268-597_47e7d21f-e346-6413-e063-6294a90aa9be", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "50268-597", "generic_name": "Nifedipine", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nifedipine", "brand_name_suffix": "ER", "active_ingredients": [{"name": "NIFEDIPINE", "strength": "30 mg/1"}], "application_number": "ANDA077127", "marketing_category": "ANDA", "marketing_start_date": "20110211", "listing_expiration_date": "20271231"}