Package 0472-1738-03

Brand: miconazole nitrate

Generic: miconazole nitrate
NDC Package

Package Facts

Identity

Package NDC 0472-1738-03
Digits Only 0472173803
Product NDC 0472-1738
Description

3 SUPPOSITORY in 1 CARTON (0472-1738-03)

Marketing

Marketing Status
Marketed Since 1995-01-18
Brand miconazole nitrate
Generic miconazole nitrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["VAGINAL"], "spl_id": "bb1aad58-4ca7-4be9-8649-0f29e22b81f5", "openfda": {"unii": ["VW4H1CYW1K"], "rxcui": ["992765"], "spl_set_id": ["aa9e250b-f317-42cb-b8d2-e85de56f4ef7"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 SUPPOSITORY in 1 CARTON (0472-1738-03)", "package_ndc": "0472-1738-03", "marketing_start_date": "19950118"}], "brand_name": "Miconazole Nitrate", "product_id": "0472-1738_bb1aad58-4ca7-4be9-8649-0f29e22b81f5", "dosage_form": "SUPPOSITORY", "pharm_class": ["Azole Antifungal [EPC]", "Azoles [CS]"], "product_ndc": "0472-1738", "generic_name": "Miconazole Nitrate", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Miconazole Nitrate", "active_ingredients": [{"name": "MICONAZOLE NITRATE", "strength": "200 mg/1"}], "application_number": "ANDA073508", "marketing_category": "ANDA", "marketing_start_date": "19950118", "listing_expiration_date": "20261231"}