Package 68788-7670-5

Brand: betamethasone dipropionate

Generic: betamethasone dipropionate
NDC Package

Package Facts

Identity

Package NDC 68788-7670-5
Digits Only 6878876705
Product NDC 68788-7670
Product ID 68788-7670_2a397c88-e201-40b5-bdfb-318e31639b25
Description

1 TUBE in 1 CARTON (68788-7670-5) / 50 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2020-02-28
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": "2a397c88-e201-40b5-bdfb-318e31639b25", "openfda": {"unii": ["826Y60901U"], "rxcui": ["848176"], "spl_set_id": ["54eff1fc-c611-4929-bb44-c1834c08f506"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (68788-7670-5)  / 50 g in 1 TUBE", "package_ndc": "68788-7670-5", "marketing_start_date": "20200228"}], "brand_name": "Betamethasone Dipropionate", "product_id": "68788-7670_2a397c88-e201-40b5-bdfb-318e31639b25", "dosage_form": "CREAM, AUGMENTED", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "68788-7670", "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": "ANDA076543", "marketing_category": "ANDA", "marketing_start_date": "20200228", "listing_expiration_date": "20261231"}