Package 62135-521-90

Brand: nifedipine

Generic: nifedipine
NDC Package

Package Facts

Identity

Package NDC 62135-521-90
Digits Only 6213552190
Product NDC 62135-521
Description

90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62135-521-90)

Marketing

Marketing Status
Marketed Since 2023-04-11
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": "462a6c34-db5b-8d31-e063-6294a90ae196", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "upc": ["0362135523909", "0362135521905", "0362135522902"], "unii": ["I9ZF7L6G2L"], "rxcui": ["1812011", "1812013", "1812015"], "spl_set_id": ["0a8e3090-7733-4914-bacb-01bbdc8deb30"], "pharm_class_cs": ["Dihydropyridines [CS]"], "pharm_class_epc": ["Dihydropyridine Calcium Channel Blocker [EPC]"], "pharm_class_moa": ["Calcium Channel Antagonists [MoA]"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62135-521-90)", "package_ndc": "62135-521-90", "marketing_start_date": "20230411"}], "brand_name": "Nifedipine", "product_id": "62135-521_462a6c34-db5b-8d31-e063-6294a90ae196", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "62135-521", "generic_name": "Nifedipine", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nifedipine", "active_ingredients": [{"name": "NIFEDIPINE", "strength": "30 mg/1"}], "application_number": "ANDA077127", "marketing_category": "ANDA", "marketing_start_date": "20051121", "listing_expiration_date": "20261231"}