Package 51672-2035-6

{"route": ["VAGINAL"], "spl_id": "362a2e22-e1bb-aae7-e063-6394a90a33f0", "openfda": {"upc": ["0351672203566"], "unii": ["VW4H1CYW1K"], "rxcui": ["998540"], "spl_set_id": ["6b34d0be-4bcd-4dff-b732-7fbd46765019"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE, WITH APPLICATOR in 1 CARTON (51672-2035-6)  / 45 g in 1 TUBE, WITH APPLICATOR", "package_ndc": "51672-2035-6", "marketing_start_date": "19970113"}, {"sample": false, "description": "1 TUBE, WITH APPLICATOR in 1 CARTON (51672-2035-7)  / 45 g in 1 TUBE, WITH APPLICATOR", "package_ndc": "51672-2035-7", "marketing_start_date": "19970113"}], "brand_name": "Miconazole Nitrate", "product_id": "51672-2035_362a2e22-e1bb-aae7-e063-6394a90a33f0", "dosage_form": "CREAM", "pharm_class": ["Azole Antifungal [EPC]", "Azoles [CS]"], "product_ndc": "51672-2035", "generic_name": "Miconazole Nitrate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Miconazole Nitrate", "active_ingredients": [{"name": "MICONAZOLE NITRATE", "strength": "20 mg/g"}], "application_number": "ANDA074444", "marketing_category": "ANDA", "marketing_start_date": "19970113", "listing_expiration_date": "20261231"}