NDC 69668-220

Deltasone

Prednisone

Deltasone is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Sonoma Pharmaceuticals, Inc.. The primary component is Prednisone.

• Product ID: 69668-220_79b342b8-58b8-c73e-e053-2a91aa0a8e28
• NDC: 69668-220
• Product Type: Human Prescription Drug
• Proprietary Name: Deltasone
• Generic Name: Prednisone
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2003-02-13
• Marketing Category: ANDA / ANDA
• Application Number: ANDA087342
• Labeler Name: Sonoma Pharmaceuticals, Inc.
• Substance Name: PREDNISONE
• Active Ingredient Strength: 20 mg/1
• Pharm Classes: Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 69668-220-20

20 TABLET in 1 BOTTLE, PLASTIC (69668-220-20)

• Marketing Start Date: 2018-11-02
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 69668-220-20 [69668022020]

Deltasone TABLET

• Marketing Category: ANDA
• Application Number: ANDA087342
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2018-11-02

Drug Details

Active Ingredients

Ingredient	Strength
PREDNISONE	20 mg/1

OpenFDA Data

• SPL SET ID: d0acd7fb-8401-424f-9acc-a74dcd9b14f6
• Manufacturer:
  • Sonoma Pharmaceuticals, Inc.
• UNII:
  • VB0R961HZT
• RxNorm Concept Unique ID - RxCUI:
  • 312615
  • 206997
• UPC Code:
  • 0369668220206

Pharmacological Class

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