Package 42291-003-30

{"route": ["ORAL"], "spl_id": "48480a71-5c94-91ab-e063-6294a90a656d", "openfda": {"upc": ["0342291003309", "0342291002302", "0342291004306", "0342291001305"], "unii": ["864V2Q084H", "6M97XTV3HD"], "rxcui": ["730861", "730866", "730869", "730872"], "spl_set_id": ["1b30c3fe-5c84-0d42-e063-6394a90a81d8"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (42291-003-30)", "package_ndc": "42291-003-30", "marketing_start_date": "20240618"}], "brand_name": "Amlodipine and Olmesartan Medoxomil", "product_id": "42291-003_48480a71-5c94-91ab-e063-6294a90a656d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A Inhibitors [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "42291-003", "generic_name": "Amlodipine and Olmesartan Medoxomil", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine and Olmesartan Medoxomil", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "10 mg/1"}, {"name": "OLMESARTAN MEDOXOMIL", "strength": "20 mg/1"}], "application_number": "ANDA209010", "marketing_category": "ANDA", "marketing_start_date": "20240618", "listing_expiration_date": "20271231"}