Package 67296-2170-1
Brand: nifedipine
Generic: nifedipinePackage Facts
Identity
Package NDC
67296-2170-1
Digits Only
6729621701
Product NDC
67296-2170
Description
14 TABLET, EXTENDED RELEASE in 1 BOTTLE (67296-2170-1)
Marketing
Marketing Status
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": "44f74622-99ed-719d-e063-6294a90ac353", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "unii": ["I9ZF7L6G2L"], "rxcui": ["198034"], "spl_set_id": ["3b0ae3ed-77ee-d0df-e063-6294a90a7d17"], "pharm_class_cs": ["Dihydropyridines [CS]"], "pharm_class_epc": ["Dihydropyridine Calcium Channel Blocker [EPC]"], "pharm_class_moa": ["Calcium Channel Antagonists [MoA]"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, EXTENDED RELEASE in 1 BOTTLE (67296-2170-1)", "package_ndc": "67296-2170-1", "marketing_start_date": "20210719"}], "brand_name": "Nifedipine", "product_id": "67296-2170_44f74622-99ed-719d-e063-6294a90ac353", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "67296-2170", "generic_name": "Nifedipine", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nifedipine", "active_ingredients": [{"name": "NIFEDIPINE", "strength": "30 mg/1"}], "application_number": "ANDA213361", "marketing_category": "ANDA", "marketing_start_date": "20210719", "listing_expiration_date": "20261231"}