Package 51672-1390-4

Brand: betamethasone dipropionate

Generic: betamethasone dipropionate
NDC Package

Package Facts

Identity

Package NDC 51672-1390-4
Digits Only 5167213904
Product NDC 51672-1390
Description

1 BOTTLE in 1 CARTON (51672-1390-4) / 60 g in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2020-06-17
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": "39628349-b360-4030-e063-6394a90a6ce9", "openfda": {"unii": ["826Y60901U"], "rxcui": ["1738536"], "spl_set_id": ["dc3dd2f7-38ad-4c4c-8602-29b33cc6af90"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (51672-1390-4)  / 60 g in 1 BOTTLE", "package_ndc": "51672-1390-4", "marketing_start_date": "20200617"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (51672-1390-8)  / 120 g in 1 BOTTLE", "package_ndc": "51672-1390-8", "marketing_start_date": "20200617"}], "brand_name": "Betamethasone dipropionate", "product_id": "51672-1390_39628349-b360-4030-e063-6394a90a6ce9", "dosage_form": "SPRAY", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "51672-1390", "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/g"}], "application_number": "ANDA211722", "marketing_category": "ANDA", "marketing_start_date": "20200617", "listing_expiration_date": "20261231"}