Package 50090-7517-0

Brand: betamethasone dipropionate

Generic: betamethasone dipropionate
NDC Package

Package Facts

Identity

Package NDC 50090-7517-0
Digits Only 5009075170
Product NDC 50090-7517
Description

50 g in 1 TUBE (50090-7517-0)

Marketing

Marketing Status
Marketed Since 2025-03-11
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": "3140f140-758c-41a6-83e2-8cb9be901863", "openfda": {"unii": ["826Y60901U"], "rxcui": ["848180"], "spl_set_id": ["018fcec3-bfb4-451c-9b54-d1fd389c2a44"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "50 g in 1 TUBE (50090-7517-0)", "package_ndc": "50090-7517-0", "marketing_start_date": "20250311"}], "brand_name": "Betamethasone Dipropionate", "product_id": "50090-7517_3140f140-758c-41a6-83e2-8cb9be901863", "dosage_form": "OINTMENT, AUGMENTED", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "50090-7517", "generic_name": "betamethasone dipropionate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Betamethasone Dipropionate", "active_ingredients": [{"name": "BETAMETHASONE DIPROPIONATE", "strength": ".5 mg/g"}], "application_number": "ANDA075373", "marketing_category": "ANDA", "marketing_start_date": "19990622", "listing_expiration_date": "20261231"}