NDC 70512-031

Diflorasone Diacetate Oint

Diflorasone Diacetate Ointment

Diflorasone Diacetate Oint is a Topical Ointment in the Human Prescription Drug category. It is labeled and distributed by Sola Pharmaceuticals. The primary component is Diflorasone Diacetate.

• Product ID: 70512-031_8383e3ec-08fb-3651-e053-2991aa0a66f6
• NDC: 70512-031
• Product Type: Human Prescription Drug
• Proprietary Name: Diflorasone Diacetate Oint
• Generic Name: Diflorasone Diacetate Ointment
• Dosage Form: Ointment
• Route of Administration: TOPICAL
• Marketing Start Date: 2019-02-04
• Marketing Category: ANDA / ANDA
• Application Number: ANDA210753
• Labeler Name: Sola Pharmaceuticals
• Substance Name: DIFLORASONE DIACETATE
• Active Ingredient Strength: 1 mg/g
• Pharm Classes: Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 70512-031-60

1 TUBE in 1 CARTON (70512-031-60) > 60 g in 1 TUBE

• Marketing Start Date: 2019-02-04
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 70512-031-60 [70512003160]

Diflorasone Diacetate Oint OINTMENT

• Marketing Category: ANDA
• Application Number: ANDA210753
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: GM
• Marketing Start Date: 2019-02-04

Drug Details

Active Ingredients

Ingredient	Strength
DIFLORASONE DIACETATE	.5 mg/g

OpenFDA Data

• SPL SET ID: 81a55188-1f73-c212-e053-2991aa0a0719
• Manufacturer:
  • Sola Pharmaceuticals
• UNII:
  • 7W2J09SCWX
• RxNorm Concept Unique ID - RxCUI:
  • 966607
• UPC Code:
  • 0370512031602

Pharmacological Class

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