NDC 70261-501

Prednisolone Acetate PF

Prednisolone Acetate Pf

Prednisolone Acetate PF is a Ophthalmic Suspension/ Drops in the Human Prescription Drug category. It is labeled and distributed by Imprimisrx Nj. The primary component is Prednisolone Acetate.

• Product ID: 70261-501_6bb6cbee-6652-7e5a-e053-2991aa0a66dd
• NDC: 70261-501
• Product Type: Human Prescription Drug
• Proprietary Name: Prednisolone Acetate PF
• Generic Name: Prednisolone Acetate Pf
• Dosage Form: Suspension/ Drops
• Route of Administration: OPHTHALMIC
• Marketing Start Date: 2018-01-01
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: ImprimisRx NJ
• Substance Name: PREDNISOLONE ACETATE
• Active Ingredient Strength: 10 mg/mL
• Pharm Classes: Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 70261-501-05

5 mL in 1 BOTTLE, DROPPER (70261-501-05)

• Marketing Start Date: 2018-01-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 70261-501-05 [70261050105]

Prednisolone Acetate PF SUSPENSION/ DROPS

• Marketing Category: unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2018-01-01
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
PREDNISOLONE ACETATE	10 mg/mL

OpenFDA Data

• SPL SET ID: 6bb6cbee-6651-7e5a-e053-2991aa0a66dd
• Manufacturer:
  • ImprimisRx NJ
• UNII:
  • 8B2807733D
• RxNorm Concept Unique ID - RxCUI:
  • 1376336

Pharmacological Class

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