Package 50090-5232-0

Brand: betamethasone dipropionate

Generic: betamethasone dipropionate
NDC Package

Package Facts

Identity

Package NDC 50090-5232-0
Digits Only 5009052320
Product NDC 50090-5232
Description

1 TUBE in 1 CARTON (50090-5232-0) / 50 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2020-10-09
Brand betamethasone dipropionate
Generic betamethasone dipropionate
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "c13a17ee-a0d4-4bed-bb51-a25dcfa26900", "openfda": {"unii": ["826Y60901U"], "rxcui": ["848176"], "spl_set_id": ["abd5a08c-4bb7-46c9-9e2e-0a89c43d46c8"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (50090-5232-0)  / 50 g in 1 TUBE", "package_ndc": "50090-5232-0", "marketing_start_date": "20201009"}], "brand_name": "Betamethasone Dipropionate", "product_id": "50090-5232_c13a17ee-a0d4-4bed-bb51-a25dcfa26900", "dosage_form": "CREAM, AUGMENTED", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "50090-5232", "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": "ANDA076543", "marketing_category": "ANDA", "marketing_start_date": "20031209", "listing_expiration_date": "20271231"}