NDC 69668-120

Deltasone

Prednisone

Deltasone is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Oculus Innovative Sciences. The primary component is Prednisone.

• Product ID: 69668-120_5d69215d-3754-782f-e053-2a91aa0a2d82
• NDC: 69668-120
• Product Type: Human Prescription Drug
• Proprietary Name: Deltasone
• Generic Name: Prednisone
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2009-08-03
• Marketing Category: ANDA / ANDA
• Application Number: ANDA083677
• Labeler Name: Oculus Innovative Sciences
• Substance Name: PREDNISONE
• Active Ingredient Strength: 20 mg/20mg
• Pharm Classes: Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 69668-120-20

20 mg in 1 BOTTLE (69668-120-20)

• Marketing Start Date: 2015-08-31
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 69668-120-20 [69668012020]

Deltasone TABLET

• Marketing Category: ANDA
• Application Number: ANDA083677
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2015-08-31
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
PREDNISONE	20 mg/20mg

OpenFDA Data

• SPL SET ID: 18bebd56-4848-32ae-e054-00144ff88e88
• Manufacturer:
  • Oculus Innovative Sciences
• UNII:
  • VB0R961HZT
• RxNorm Concept Unique ID - RxCUI:
  • 312615
  • 206997

Pharmacological Class

• Corticosteroid [EPC]
• Corticosteroid Hormone Receptor Agonists [MoA]

NDC Crossover Matching brand name "Deltasone" or generic name "Prednisone"

NDC	Brand Name	Generic Name
69668-220	Deltasone	Deltasone
69668-120	Deltasone	Deltasone
0054-0017	PredniSONE	PredniSONE
0054-0018	PredniSONE	PredniSONE
0054-0019	PredniSONE	PredniSONE
0054-3722	PredniSONE	PredniSONE
0054-4728	PredniSONE	PredniSONE
0054-4741	PredniSONE	PredniSONE