Label: DELTASONE- prednisone tablet
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Contains inactivated NDC Code(s)
NDC Code(s): 69668-120-20 - Packager: Oculus Innovative Sciences
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated November 7, 2017
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
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Warnings
Warnings: Keep this product out of reach
of children. In case of accidental overdose,
call a doctor or poison control center
immediately.
All prescriptions using this product shall be
pursuant to state statutes as applicable.
This product may be administered only
under a physician’s supervision.
Call your doctor about side effects.
You may report side effects to FDA at
1-800-FDA-1088. - Deltasone 20mg
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INGREDIENTS AND APPEARANCE
DELTASONE
prednisone tabletProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:69668-120 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PREDNISONE (UNII: VB0R961HZT) (PREDNISONE - UNII:VB0R961HZT) PREDNISONE 20 mg in 20 mg Product Characteristics Color orange Score 2 pieces Shape ROUND Size 9mm Flavor Imprint Code Westward;477 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69668-120-20 20 mg in 1 BOTTLE; Type 0: Not a Combination Product 08/31/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA083677 08/03/2009 Labeler - Oculus Innovative Sciences (081642964)