Package 45802-021-46

Brand: betamethasone dipropionate

Generic: betamethasone dipropionate
NDC Package

Package Facts

Identity

Package NDC 45802-021-46
Digits Only 4580202146
Product NDC 45802-021
Description

56.2 g in 1 BOTTLE, PLASTIC (45802-021-46)

Marketing

Marketing Status
Marketed Since 2006-06-30
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": "2957986c-340c-4ef1-b78d-08b119fa703b", "openfda": {"unii": ["826Y60901U"], "rxcui": ["240209"], "spl_set_id": ["e6018480-7788-472d-a2d1-ccccffcd258e"], "manufacturer_name": ["Padagis Israel Pharmaceuticals Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "56.2 g in 1 BOTTLE, PLASTIC (45802-021-46)", "package_ndc": "45802-021-46", "marketing_start_date": "20060630"}], "brand_name": "Betamethasone Dipropionate", "product_id": "45802-021_2957986c-340c-4ef1-b78d-08b119fa703b", "dosage_form": "LOTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "45802-021", "generic_name": "Betamethasone Dipropionate", "labeler_name": "Padagis Israel Pharmaceuticals Ltd", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Betamethasone Dipropionate", "active_ingredients": [{"name": "BETAMETHASONE DIPROPIONATE", "strength": ".5 mg/g"}], "application_number": "ANDA072538", "marketing_category": "ANDA", "marketing_start_date": "20060630", "listing_expiration_date": "20261231"}