Package 0472-0382-45

Brand: betamethasone dipropionate

Generic: betamethasone dipropionate
NDC Package

Package Facts

Identity

Package NDC 0472-0382-45
Digits Only 0472038245
Product NDC 0472-0382
Product ID 0472-0382_2f2016cb-8b63-40ef-ad6d-4850179ec8cd
Description

1 TUBE in 1 CARTON (0472-0382-45) / 45 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 1995-09-01
Brand betamethasone dipropionate
Generic betamethasone dipropionate
Sample Package No

Linked Drug Pages (1)

Betamethasone Dipropionate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "2f2016cb-8b63-40ef-ad6d-4850179ec8cd", "openfda": {"unii": ["826Y60901U"], "rxcui": ["848180"], "spl_set_id": ["af8317d7-b280-4f40-ad88-802f99d33d78"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (0472-0382-15)  / 15 g in 1 TUBE", "package_ndc": "0472-0382-15", "marketing_start_date": "19950901"}, {"sample": false, "description": "1 TUBE in 1 CARTON (0472-0382-45)  / 45 g in 1 TUBE", "package_ndc": "0472-0382-45", "marketing_start_date": "19950901"}], "brand_name": "Betamethasone Dipropionate", "product_id": "0472-0382_2f2016cb-8b63-40ef-ad6d-4850179ec8cd", "dosage_form": "OINTMENT, AUGMENTED", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "0472-0382", "generic_name": "Betamethasone Dipropionate", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Betamethasone Dipropionate", "active_ingredients": [{"name": "BETAMETHASONE DIPROPIONATE", "strength": ".5 mg/g"}], "application_number": "ANDA074304", "marketing_category": "ANDA", "marketing_start_date": "19950901", "listing_expiration_date": "20261231"}