Package 51672-1310-1

{"route": ["TOPICAL"], "spl_id": "3fb723a8-70e1-d700-e063-6294a90a53c5", "openfda": {"unii": ["826Y60901U"], "rxcui": ["848176"], "spl_set_id": ["000ae256-a337-4903-845b-003777a4efa8"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (51672-1310-1)  / 15 g in 1 TUBE", "package_ndc": "51672-1310-1", "marketing_start_date": "20031209"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-1310-2)  / 30 g in 1 TUBE", "package_ndc": "51672-1310-2", "marketing_start_date": "20031209"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-1310-3)  / 50 g in 1 TUBE", "package_ndc": "51672-1310-3", "marketing_start_date": "20031209"}], "brand_name": "Betamethasone Dipropionate", "product_id": "51672-1310_3fb723a8-70e1-d700-e063-6294a90a53c5", "dosage_form": "CREAM, AUGMENTED", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "51672-1310", "generic_name": "Betamethasone Dipropionate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Betamethasone Dipropionate", "active_ingredients": [{"name": "BETAMETHASONE DIPROPIONATE", "strength": ".5 mg/g"}], "application_number": "ANDA076543", "marketing_category": "ANDA", "marketing_start_date": "20031209", "listing_expiration_date": "20261231"}