Package 43063-764-30

Brand: amlodipine besylate

Generic: amlodipine besylate
NDC Package

Package Facts

Identity

Package NDC 43063-764-30
Digits Only 4306376430
Product NDC 43063-764
Description

30 TABLET in 1 BOTTLE, PLASTIC (43063-764-30)

Marketing

Marketing Status
Marketed Since 2017-05-08
Brand amlodipine besylate
Generic amlodipine besylate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47d29cab-fc5f-977d-e063-6294a90a6bf1", "openfda": {"upc": ["0343063764305"], "unii": ["864V2Q084H"], "rxcui": ["308136"], "spl_set_id": ["e01efe66-2f31-4261-92ca-0b41f27104da"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-764-30)", "package_ndc": "43063-764-30", "marketing_start_date": "20170508"}], "brand_name": "AMLODIPINE BESYLATE", "product_id": "43063-764_47d29cab-fc5f-977d-e063-6294a90a6bf1", "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": "43063-764", "generic_name": "AMLODIPINE BESYLATE", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMLODIPINE BESYLATE", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "2.5 mg/1"}], "application_number": "ANDA077073", "marketing_category": "ANDA", "marketing_start_date": "20070926", "listing_expiration_date": "20271231"}