Package 70518-4187-0

Brand: betamethasone dipropionate

Generic: betamethasone dipropionate
NDC Package

Package Facts

Identity

Package NDC 70518-4187-0
Digits Only 7051841870
Product NDC 70518-4187
Description

1 TUBE in 1 CARTON (70518-4187-0) / 15 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2024-09-26
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": "3ff28b03-c91e-4df8-e063-6294a90a52a8", "openfda": {"unii": ["826Y60901U"], "rxcui": ["238920"], "spl_set_id": ["7cacf0ec-3db9-48be-9a76-93ed4a1f042c"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (70518-4187-0)  / 15 g in 1 TUBE", "package_ndc": "70518-4187-0", "marketing_start_date": "20240926"}], "brand_name": "Betamethasone Dipropionate", "product_id": "70518-4187_3ff28b03-c91e-4df8-e063-6294a90a52a8", "dosage_form": "CREAM", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "70518-4187", "generic_name": "Betamethasone Dipropionate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Betamethasone Dipropionate", "active_ingredients": [{"name": "BETAMETHASONE DIPROPIONATE", "strength": ".5 mg/g"}], "application_number": "NDA019137", "marketing_category": "NDA", "marketing_start_date": "20240926", "listing_expiration_date": "20261231"}