Package 51672-1309-3
Brand: betamethasone dipropionate
Generic: betamethasone dipropionatePackage 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
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"}