Package 0472-0381-45

Brand: betamethasone dipropionate

Generic: betamethasone dipropionate
NDC Package

Package Facts

Identity

Package NDC 0472-0381-45
Digits Only 0472038145
Product NDC 0472-0381
Description

1 TUBE in 1 CARTON (0472-0381-45) / 45 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 1997-02-01
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": "e8e8285a-02b1-4e44-baf1-459545f7a631", "openfda": {"unii": ["826Y60901U"], "rxcui": ["197405"], "spl_set_id": ["aa3f4012-7597-422d-8bcc-00102780a152"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (0472-0381-15)  / 15 g in 1 TUBE", "package_ndc": "0472-0381-15", "marketing_start_date": "19970201"}, {"sample": false, "description": "1 TUBE in 1 CARTON (0472-0381-45)  / 45 g in 1 TUBE", "package_ndc": "0472-0381-45", "marketing_start_date": "19970201"}], "brand_name": "Betamethasone Dipropionate", "product_id": "0472-0381_e8e8285a-02b1-4e44-baf1-459545f7a631", "dosage_form": "OINTMENT", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "0472-0381", "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": "ANDA071012", "marketing_category": "ANDA", "marketing_start_date": "19970201", "listing_expiration_date": "20261231"}