Package 50742-621-01

Brand: nifedipine

Generic: nifedipine
NDC Package

Package Facts

Identity

Package NDC 50742-621-01
Digits Only 5074262101
Product NDC 50742-621
Product ID 50742-621_5d0a8a20-c19f-43b1-a124-ba6f5bc99f3a
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-621-01)

Marketing

Marketing Status
Marketed Since 2017-02-15
Brand nifedipine
Generic nifedipine
Sample Package No

Linked Drug Pages (1)

Nifedipine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5d0a8a20-c19f-43b1-a124-ba6f5bc99f3a", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "unii": ["I9ZF7L6G2L"], "rxcui": ["198034", "198035", "198036"], "spl_set_id": ["4d02eba2-e964-4fa7-aaae-25949b5f0316"], "pharm_class_cs": ["Dihydropyridines [CS]"], "pharm_class_epc": ["Dihydropyridine Calcium Channel Blocker [EPC]"], "pharm_class_moa": ["Calcium Channel Antagonists [MoA]"], "manufacturer_name": ["Ingenus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-621-01)", "package_ndc": "50742-621-01", "marketing_start_date": "20170215"}], "brand_name": "Nifedipine", "product_id": "50742-621_5d0a8a20-c19f-43b1-a124-ba6f5bc99f3a", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "50742-621", "generic_name": "nifedipine", "labeler_name": "Ingenus Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nifedipine", "active_ingredients": [{"name": "NIFEDIPINE", "strength": "60 mg/1"}], "application_number": "ANDA202987", "marketing_category": "ANDA", "marketing_start_date": "20170215", "listing_expiration_date": "20261231"}