Package 60760-614-30

Brand: amlodipine besylate

Generic: amlodipine besylate
NDC Package

Package Facts

Identity

Package NDC 60760-614-30
Digits Only 6076061430
Product NDC 60760-614
Product ID 60760-614_cdb68210-952f-e8da-e053-2a95a90aec7e
Description

30 TABLET in 1 BOTTLE, PLASTIC (60760-614-30)

Marketing

Marketing Status
Marketed Since 2021-09-23
Brand amlodipine besylate
Generic amlodipine besylate
Sample Package No

Linked Drug Pages (1)

Amlodipine Besylate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "cdb68210-952f-e8da-e053-2a95a90aec7e", "openfda": {"unii": ["864V2Q084H"], "rxcui": ["308135"], "spl_set_id": ["cdb68210-952e-e8da-e053-2a95a90aec7e"], "manufacturer_name": ["St. Mary's Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (60760-614-30)", "package_ndc": "60760-614-30", "marketing_start_date": "20210923"}], "brand_name": "Amlodipine Besylate", "product_id": "60760-614_cdb68210-952f-e8da-e053-2a95a90aec7e", "dosage_form": "TABLET", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "60760-614", "generic_name": "Amlodipine besylate", "labeler_name": "St. Mary's Medical Park Pharmacy", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine Besylate", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "10 mg/1"}], "application_number": "ANDA078925", "marketing_category": "ANDA", "marketing_start_date": "20210923", "listing_expiration_date": "20261231"}