Package 71205-275-15

Brand: betamethasone dipropionate

Generic: betamethasone dipropionate
NDC Package

Package Facts

Identity

Package NDC 71205-275-15
Digits Only 7120527515
Product NDC 71205-275
Description

1 TUBE in 1 CARTON (71205-275-15) / 15 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2019-05-01
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": "c1b9e3e4-cd76-4429-94c9-4ea082f0ad8b", "openfda": {"upc": ["0371205275150"], "unii": ["826Y60901U"], "rxcui": ["848176"], "spl_set_id": ["f1be7c91-5408-4d31-8673-b691089aadce"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (71205-275-15)  / 15 g in 1 TUBE", "package_ndc": "71205-275-15", "marketing_start_date": "20190501"}], "brand_name": "Betamethasone Dipropionate", "product_id": "71205-275_c1b9e3e4-cd76-4429-94c9-4ea082f0ad8b", "dosage_form": "CREAM", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "71205-275", "generic_name": "Betamethasone Dipropionate", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Betamethasone Dipropionate", "active_ingredients": [{"name": "BETAMETHASONE DIPROPIONATE", "strength": ".5 mg/g"}], "application_number": "ANDA076592", "marketing_category": "ANDA", "marketing_start_date": "20060928", "listing_expiration_date": "20261231"}