Package 71205-122-30

Brand: amlodipine and benazepril hydrochloride

Generic: amlodipine and benazepril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71205-122-30
Digits Only 7120512230
Product NDC 71205-122
Description

30 CAPSULE in 1 BOTTLE (71205-122-30)

Marketing

Marketing Status
Marketed Since 2018-09-04
Brand amlodipine and benazepril hydrochloride
Generic amlodipine and benazepril hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5a8c9c91-d6eb-4f0d-bbc7-3ccab08accff", "openfda": {"upc": ["0371205122300"], "unii": ["864V2Q084H", "N1SN99T69T"], "rxcui": ["898356"], "spl_set_id": ["29a0d87e-6afb-4766-9045-1963c5b0d183"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (71205-122-30)", "package_ndc": "71205-122-30", "marketing_start_date": "20180904"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (71205-122-60)", "package_ndc": "71205-122-60", "marketing_start_date": "20180904"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (71205-122-90)", "package_ndc": "71205-122-90", "marketing_start_date": "20180904"}], "brand_name": "Amlodipine and Benazepril Hydrochloride", "product_id": "71205-122_5a8c9c91-d6eb-4f0d-bbc7-3ccab08accff", "dosage_form": "CAPSULE", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A Inhibitors [MoA]", "Decreased Blood Pressure [PE]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "71205-122", "generic_name": "Amlodipine and Benazepril Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine and Benazepril Hydrochloride", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "5 mg/1"}, {"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA202239", "marketing_category": "ANDA", "marketing_start_date": "20120905", "listing_expiration_date": "20261231"}