Package 51672-1362-8

{"route": ["TOPICAL"], "spl_id": "39620da3-e660-e94f-e063-6294a90afd69", "openfda": {"unii": ["25UR9N9041"], "rxcui": ["896110"], "spl_set_id": ["d50961c2-e97f-4583-91d6-7cafd25a8c3d"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (51672-1362-1)  / 15 g in 1 TUBE", "package_ndc": "51672-1362-1", "marketing_start_date": "20160908"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-1362-2)  / 30 g in 1 TUBE", "package_ndc": "51672-1362-2", "marketing_start_date": "20160908"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-1362-3)  / 60 g in 1 TUBE", "package_ndc": "51672-1362-3", "marketing_start_date": "20160908"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-1362-8)  / 90 g in 1 TUBE", "package_ndc": "51672-1362-8", "marketing_start_date": "20160908"}], "brand_name": "Naftifine Hydrochloride", "product_id": "51672-1362_39620da3-e660-e94f-e063-6294a90afd69", "dosage_form": "CREAM", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "51672-1362", "generic_name": "Naftifine Hydrochloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naftifine Hydrochloride", "active_ingredients": [{"name": "NAFTIFINE HYDROCHLORIDE", "strength": "10 mg/g"}], "application_number": "ANDA205975", "marketing_category": "ANDA", "marketing_start_date": "20160908", "listing_expiration_date": "20261231"}