Package 51672-1340-3

Brand: betamethasone dipropionate

Generic: betamethasone dipropionate
NDC Package

Package Facts

Identity

Package NDC 51672-1340-3
Digits Only 5167213403
Product NDC 51672-1340
Description

1 BOTTLE in 1 CARTON (51672-1340-3) / 30 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2007-05-21
Brand betamethasone dipropionate
Generic betamethasone dipropionate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "3961e128-73c9-c458-e063-6294a90a8a8f", "openfda": {"unii": ["826Y60901U"], "rxcui": ["848178"], "spl_set_id": ["3b23a3c0-3306-4a2d-932d-25916d16dc68"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (51672-1340-3)  / 30 mL in 1 BOTTLE", "package_ndc": "51672-1340-3", "marketing_start_date": "20070521"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (51672-1340-4)  / 60 mL in 1 BOTTLE", "package_ndc": "51672-1340-4", "marketing_start_date": "20070521"}], "brand_name": "Betamethasone Dipropionate", "product_id": "51672-1340_3961e128-73c9-c458-e063-6294a90a8a8f", "dosage_form": "LOTION, AUGMENTED", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "51672-1340", "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/mL"}], "application_number": "ANDA077477", "marketing_category": "ANDA", "marketing_start_date": "20070521", "listing_expiration_date": "20261231"}