Package 42708-066-30

Brand: amlodipine besylate

Generic: amlodipine besylate
NDC Package Sample

Package Facts

Identity

Package NDC 42708-066-30
Digits Only 4270806630
Product NDC 42708-066
Product ID 42708-066_45b3d5c6-5c65-777f-e063-6294a90a58a5
Description

30 TABLET in 1 BOTTLE (42708-066-30)

Marketing

Marketing Status
Marketed Since 2018-08-16
Brand amlodipine besylate
Generic amlodipine besylate
Sample Package Yes

Linked Drug Pages (1)

Amlodipine Besylate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "45b3d5c6-5c65-777f-e063-6294a90a58a5", "openfda": {"unii": ["864V2Q084H"], "rxcui": ["197361"], "spl_set_id": ["3f74ed2b-4712-4026-ac2c-9239a211dde3"], "manufacturer_name": ["QPharma Inc"]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET in 1 BOTTLE (42708-066-30)", "package_ndc": "42708-066-30", "marketing_start_date": "20180816"}], "brand_name": "Amlodipine Besylate", "product_id": "42708-066_45b3d5c6-5c65-777f-e063-6294a90a58a5", "dosage_form": "TABLET", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A Inhibitors [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "42708-066", "generic_name": "Amlodipine besylate", "labeler_name": "QPharma Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine Besylate", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "5 mg/1"}], "application_number": "ANDA078925", "marketing_category": "ANDA", "marketing_start_date": "20101020", "listing_expiration_date": "20261231"}