Package 51672-1390-4
Brand: betamethasone dipropionate
Generic: betamethasone dipropionatePackage 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
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"}