Package 0069-2650-66
Brand: procardia xl
Generic: nifedipinePackage Facts
Identity
Package NDC
0069-2650-66
Digits Only
0069265066
Product NDC
0069-2650
Description
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0069-2650-66)
Marketing
Marketing Status
Brand
procardia xl
Generic
nifedipine
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c24a0478-46d4-413a-8d48-c21af0bc10e4", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "unii": ["I9ZF7L6G2L"], "rxcui": ["207772", "207773", "207774", "1812011", "1812013", "1812015"], "spl_set_id": ["8ebcb33c-f43b-4b36-9f94-9774b2a59e06"], "pharm_class_cs": ["Dihydropyridines [CS]"], "pharm_class_epc": ["Dihydropyridine Calcium Channel Blocker [EPC]"], "pharm_class_moa": ["Calcium Channel Antagonists [MoA]"], "manufacturer_name": ["Pfizer Laboratories Div Pfizer Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0069-2650-41)", "package_ndc": "0069-2650-41", "marketing_start_date": "19890906"}, {"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0069-2650-66)", "package_ndc": "0069-2650-66", "marketing_start_date": "19890906"}, {"sample": false, "description": "300 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0069-2650-72)", "package_ndc": "0069-2650-72", "marketing_start_date": "19890906"}], "brand_name": "Procardia XL", "product_id": "0069-2650_c24a0478-46d4-413a-8d48-c21af0bc10e4", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "0069-2650", "generic_name": "nifedipine", "labeler_name": "Pfizer Laboratories Div Pfizer Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Procardia", "brand_name_suffix": "XL", "active_ingredients": [{"name": "NIFEDIPINE", "strength": "30 mg/1"}], "application_number": "NDA019684", "marketing_category": "NDA", "marketing_start_date": "19890906", "listing_expiration_date": "20261231"}