Package 51672-2070-9

Brand: miconazole nitrate

Generic: miconazole nitrate
NDC Package

Package Facts

Identity

Package NDC 51672-2070-9
Digits Only 5167220709
Product NDC 51672-2070
Product ID 51672-2070_38e566b7-9252-2731-e063-6294a90ad263
Description

1 TUBE, WITH APPLICATOR in 1 CARTON (51672-2070-9) / 25 g in 1 TUBE, WITH APPLICATOR

Marketing

Marketing Status
Marketed Since 2005-03-02
Brand miconazole nitrate
Generic miconazole nitrate
Sample Package No

Linked Drug Pages (1)

Miconazole Nitrate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["VAGINAL"], "spl_id": "38e566b7-9252-2731-e063-6294a90ad263", "openfda": {"unii": ["VW4H1CYW1K"], "rxcui": ["998544"], "spl_set_id": ["eaca3e39-6ea0-4d7e-803c-db22024ad9f9"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE, WITH APPLICATOR in 1 CARTON (51672-2070-9)  / 25 g in 1 TUBE, WITH APPLICATOR", "package_ndc": "51672-2070-9", "marketing_start_date": "20050302"}], "brand_name": "Miconazole Nitrate", "product_id": "51672-2070_38e566b7-9252-2731-e063-6294a90ad263", "dosage_form": "CREAM", "pharm_class": ["Azole Antifungal [EPC]", "Azoles [CS]"], "product_ndc": "51672-2070", "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": "40 mg/g"}], "application_number": "ANDA076773", "marketing_category": "ANDA", "marketing_start_date": "20050302", "listing_expiration_date": "20261231"}