Package 51672-1309-3

Brand: betamethasone dipropionate

Generic: betamethasone dipropionate
NDC Package

Package Facts

Identity

Package NDC 51672-1309-3
Digits Only 5167213093
Product NDC 51672-1309
Description

1 TUBE in 1 CARTON (51672-1309-3) / 50 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2003-12-02
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": "38f65f63-5416-f33d-e063-6294a90a4238", "openfda": {"unii": ["826Y60901U"], "rxcui": ["848208"], "spl_set_id": ["e041ceb2-8bda-4703-b663-804e7b462e32"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (51672-1309-1)  / 15 g in 1 TUBE", "package_ndc": "51672-1309-1", "marketing_start_date": "20031202"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-1309-3)  / 50 g in 1 TUBE", "package_ndc": "51672-1309-3", "marketing_start_date": "20031202"}], "brand_name": "Betamethasone Dipropionate", "product_id": "51672-1309_38f65f63-5416-f33d-e063-6294a90a4238", "dosage_form": "GEL", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "51672-1309", "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": "ANDA076508", "marketing_category": "ANDA", "marketing_start_date": "20031202", "listing_expiration_date": "20261231"}