Deltasone
Deltasone 20mg prednisone tablets
Approved
Approval ID
18bebd56-4848-32ae-e054-00144ff88e88
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 7, 2017
Manufacturers
FDA
Oculus Innovative Sciences
DUNS: 081642964
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Prednisone
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code69668-120
Application NumberANDA083677
Product Classification
M
Marketing Category
C73584
G
Generic Name
Prednisone
Product Specifications
Route of AdministrationORAL
Effective DateNovember 7, 2017
FDA Product Classification
INGREDIENTS (1)
PREDNISONEActive
Quantity: 20 mg in 20 mg
Code: VB0R961HZT
Classification: ACTIB