Package 51672-1274-6

Brand: betamethasone dipropionate

Generic: betamethasone dipropionate
NDC Package

Package Facts

Identity

Package NDC 51672-1274-6
Digits Only 5167212746
Product NDC 51672-1274
Description

1 TUBE in 1 CARTON (51672-1274-6) / 45 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 1992-04-30
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": "38f55e1e-dffd-ee76-e063-6394a90aee5e", "openfda": {"unii": ["826Y60901U"], "rxcui": ["238920"], "spl_set_id": ["bc12c828-54ba-411d-b752-9b735f7adf63"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (51672-1274-1)  / 15 g in 1 TUBE", "package_ndc": "51672-1274-1", "marketing_start_date": "19920430"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-1274-6)  / 45 g in 1 TUBE", "package_ndc": "51672-1274-6", "marketing_start_date": "19920430"}], "brand_name": "Betamethasone Dipropionate", "product_id": "51672-1274_38f55e1e-dffd-ee76-e063-6394a90aee5e", "dosage_form": "CREAM", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "51672-1274", "generic_name": "Betamethasone Dipropionate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Betamethasone Dipropionate", "active_ingredients": [{"name": "BETAMETHASONE DIPROPIONATE", "strength": ".5 mg/g"}], "application_number": "ANDA073552", "marketing_category": "ANDA", "marketing_start_date": "19920430", "listing_expiration_date": "20261231"}