Package 0713-0807-53

Brand: betamethasone dipropionate

Generic: betamethasone dipropionate
NDC Package

Package Facts

Identity

Package NDC 0713-0807-53
Digits Only 0713080753
Product NDC 0713-0807
Description

1 BOTTLE in 1 CARTON (0713-0807-53) / 60 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2016-09-05
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": "ed81406a-8c03-5c33-e053-2a95a90a941f", "openfda": {"upc": ["0307130807531"], "unii": ["826Y60901U"], "rxcui": ["240209"], "spl_set_id": ["c9839c0a-bee5-0ef7-8933-e6231c440407"], "manufacturer_name": ["Cosette Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0713-0807-53)  / 60 mL in 1 BOTTLE", "package_ndc": "0713-0807-53", "marketing_start_date": "20160905"}], "brand_name": "Betamethasone Dipropionate", "product_id": "0713-0807_ed81406a-8c03-5c33-e053-2a95a90a941f", "dosage_form": "LOTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "0713-0807", "generic_name": "Betamethasone Dipropionate", "labeler_name": "Cosette Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Betamethasone Dipropionate", "active_ingredients": [{"name": "BETAMETHASONE DIPROPIONATE", "strength": ".5 mg/mL"}], "application_number": "ANDA071467", "marketing_category": "ANDA", "marketing_start_date": "20160905", "listing_expiration_date": "20261231"}