NDC 0023-0066

PRED-G

Gentamicin Sulfate And Prednisolone Acetate

PRED-G is a Ophthalmic Ointment in the Human Prescription Drug category. It is labeled and distributed by Allergan, Inc.. The primary component is Gentamicin Sulfate; Prednisolone Acetate.

• Product ID: 0023-0066_05f7c3fc-cc93-49c4-8e82-16bd49d79d73
• NDC: 0023-0066
• Product Type: Human Prescription Drug
• Proprietary Name: PRED-G
• Generic Name: Gentamicin Sulfate And Prednisolone Acetate
• Dosage Form: Ointment
• Route of Administration: OPHTHALMIC
• Marketing Start Date: 1990-01-01
• Marketing Category: NDA / NDA
• Application Number: NDA050612
• Labeler Name: Allergan, Inc.
• Substance Name: GENTAMICIN SULFATE; PREDNISOLONE ACETATE
• Active Ingredient Strength: 3 mg/g; mg/g
• Pharm Classes: Aminoglycoside Antibacterial [EPC], Aminoglycosides [CS], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 0023-0066-04

1 TUBE in 1 CARTON (0023-0066-04) > 3.5 g in 1 TUBE

• Marketing Start Date: 1990-01-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0023-0066-04 [00023006604]

PRED-G OINTMENT

• Marketing Category: NDA
• Application Number: NDA050612
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: GM
• Marketing Start Date: 1990-01-01

Drug Details

Active Ingredients

Ingredient	Strength
GENTAMICIN SULFATE	3 mg/g

OpenFDA Data

• SPL SET ID: a76fce5c-81b4-4fa6-904b-34c2313a0828
• Manufacturer:
  • Allergan, Inc.
• UNII:
  • 8X7386QRLV
  • 8B2807733D
• RxNorm Concept Unique ID - RxCUI:
  • 310468
  • 260285

Pharmacological Class

• Aminoglycoside Antibacterial [EPC]
• Aminoglycosides [CS]
• Corticosteroid [EPC]
• Corticosteroid Hormone Receptor Agonists [MoA]

NDC Crossover Matching brand name "PRED-G" or generic name "Gentamicin Sulfate And Prednisolone Acetate"

NDC	Brand Name	Generic Name
0023-0066	PRED-G	gentamicin sulfate and prednisolone acetate
0023-0106	PRED-G	gentamicin, prednisolone acetate