Home > National Drug Code (NDC) > Betamethasone Dipropionate

Betamethasone Dipropionate - 49999-222-15 - (Betamethasone Dipropionate)

Alphabetical Index


Drug Information of Betamethasone Dipropionate

Product NDC: 49999-222
Proprietary Name: Betamethasone Dipropionate
Non Proprietary Name: Betamethasone Dipropionate
Active Ingredient(s): .5    mg/g & nbsp;   Betamethasone Dipropionate
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Betamethasone Dipropionate

Product NDC: 49999-222
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA019137
Marketing Category: ANDA
Start Marketing Date: 20120326

Package Information of Betamethasone Dipropionate

Package NDC: 49999-222-15
Package Description: 1 TUBE in 1 CARTON (49999-222-15) > 15 g in 1 TUBE

NDC Information of Betamethasone Dipropionate

NDC Code 49999-222-15
Proprietary Name Betamethasone Dipropionate
Package Description 1 TUBE in 1 CARTON (49999-222-15) > 15 g in 1 TUBE
Product NDC 49999-222
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Betamethasone Dipropionate
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20120326
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name BETAMETHASONE DIPROPIONATE
Strength Number .5
Strength Unit mg/g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Betamethasone Dipropionate


General Information