Package 71335-2129-2

{"route": ["ORAL"], "spl_id": "c4a7d0d5-55fa-4737-9d68-83466e5b83ac", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["830861"], "spl_set_id": ["22e653e5-4122-4d7d-b9ad-0bdc1390fb40"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-2129-1)", "package_ndc": "71335-2129-1", "marketing_start_date": "20220804"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-2129-2)", "package_ndc": "71335-2129-2", "marketing_start_date": "20220719"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "71335-2129_c4a7d0d5-55fa-4737-9d68-83466e5b83ac", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "71335-2129", "generic_name": "Diltiazem hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA205231", "marketing_category": "ANDA", "marketing_start_date": "20181001", "listing_expiration_date": "20261231"}