Package 68788-9219-1

Brand: betamethasone dipropionate

Generic: betamethasone dipropionate
NDC Package

Package Facts

Identity

Package NDC 68788-9219-1
Digits Only 6878892191
Product NDC 68788-9219
Product ID 68788-9219_6ea43bf4-ed8c-450d-a774-0e2259654baa
Description

1 TUBE in 1 CARTON (68788-9219-1) / 15 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2014-09-19
Brand betamethasone dipropionate
Generic betamethasone dipropionate
Sample Package No

Linked Drug Pages (1)

Betamethasone Dipropionate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "6ea43bf4-ed8c-450d-a774-0e2259654baa", "openfda": {"unii": ["826Y60901U"], "rxcui": ["848176"], "spl_set_id": ["5683885d-461c-4e7e-bbe8-dc231d706192"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (68788-9219-1)  / 15 g in 1 TUBE", "package_ndc": "68788-9219-1", "marketing_start_date": "20140919"}], "brand_name": "Betamethasone Dipropionate", "product_id": "68788-9219_6ea43bf4-ed8c-450d-a774-0e2259654baa", "dosage_form": "CREAM", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "68788-9219", "generic_name": "Betamethasone Dipropionate", "labeler_name": "Preferred Pharmaceuticals, Inc.", "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": "20140919", "listing_expiration_date": "20261231"}