Package 0168-0267-30

Brand: betamethasone dipropionate

Generic: betamethasone dipropionate
NDC Package

Package Facts

Identity

Package NDC 0168-0267-30
Digits Only 0168026730
Product NDC 0168-0267
Product ID 0168-0267_5d745268-8539-4108-a0eb-444a4b1424b9
Description

30 mL in 1 BOTTLE (0168-0267-30)

Marketing

Marketing Status
Marketed Since 2007-05-21
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": "5d745268-8539-4108-a0eb-444a4b1424b9", "openfda": {"unii": ["826Y60901U"], "rxcui": ["848178"], "spl_set_id": ["4f411e41-00dc-47cf-8517-3ff5876e1bf5"], "manufacturer_name": ["E. Fougera & Co. a division of Fougera Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 BOTTLE (0168-0267-30)", "package_ndc": "0168-0267-30", "marketing_start_date": "20070521"}, {"sample": false, "description": "60 mL in 1 BOTTLE (0168-0267-60)", "package_ndc": "0168-0267-60", "marketing_start_date": "20070521"}], "brand_name": "Betamethasone Dipropionate", "product_id": "0168-0267_5d745268-8539-4108-a0eb-444a4b1424b9", "dosage_form": "LOTION, AUGMENTED", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "0168-0267", "generic_name": "Betamethasone Dipropionate", "labeler_name": "E. Fougera & Co. a division of Fougera Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Betamethasone Dipropionate", "active_ingredients": [{"name": "BETAMETHASONE DIPROPIONATE", "strength": ".5 mg/mL"}], "application_number": "ANDA077111", "marketing_category": "ANDA", "marketing_start_date": "20070521", "listing_expiration_date": "20271231"}