Package 62332-784-71

{"route": ["ORAL"], "spl_id": "2180c38c-9155-4c89-83c0-ea9e0bb568fb", "openfda": {"upc": ["0362332781317", "0362332782314"], "unii": ["OLH94387TE"], "rxcui": ["831054", "831102", "831103", "833217"], "spl_set_id": ["ab38794a-914d-4bcd-9c6d-1578aa10041a"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (62332-784-31)", "package_ndc": "62332-784-31", "marketing_start_date": "20251114"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (62332-784-71)", "package_ndc": "62332-784-71", "marketing_start_date": "20251114"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "62332-784_2180c38c-9155-4c89-83c0-ea9e0bb568fb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "62332-784", "generic_name": "Diltiazem Hydrochloride", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA217633", "marketing_category": "ANDA", "marketing_start_date": "20251114", "listing_expiration_date": "20261231"}