Package 63629-8613-1

Brand: betamethasone dipropionate

Generic: betamethasone dipropionate
NDC Package

Package Facts

Identity

Package NDC 63629-8613-1
Digits Only 6362986131
Product NDC 63629-8613
Description

1 TUBE in 1 CARTON (63629-8613-1) / 15 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2021-07-09
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": "bb35a5f9-bda6-49bd-88a4-4681c540cda3", "openfda": {"unii": ["826Y60901U"], "rxcui": ["848176"], "spl_set_id": ["0481ac0d-9220-472b-b3f2-af6e0bb6962d"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (63629-8613-1)  / 15 g in 1 TUBE", "package_ndc": "63629-8613-1", "marketing_start_date": "20210709"}], "brand_name": "Betamethasone Dipropionate", "product_id": "63629-8613_bb35a5f9-bda6-49bd-88a4-4681c540cda3", "dosage_form": "CREAM", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "63629-8613", "generic_name": "Betamethasone Dipropionate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Betamethasone Dipropionate", "active_ingredients": [{"name": "BETAMETHASONE DIPROPIONATE", "strength": ".5 mg/g"}], "application_number": "ANDA076592", "marketing_category": "ANDA", "marketing_start_date": "20060928", "listing_expiration_date": "20261231"}