NDC 54799-503

GONIOSOFT

Hypromellose 2.5%

GONIOSOFT is a Ophthalmic Liquid in the Human Otc Drug category. It is labeled and distributed by Ocusoft, Inc.. The primary component is Hypromelloses.

• Product ID: 54799-503_6a367c59-f113-454e-97ae-bd404cd3d32e
• NDC: 54799-503
• Product Type: Human Otc Drug
• Proprietary Name: GONIOSOFT
• Generic Name: Hypromellose 2.5%
• Dosage Form: Liquid
• Route of Administration: OPHTHALMIC
• Marketing Start Date: 1989-10-02
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: OCuSOFT, Inc.
• Substance Name: HYPROMELLOSES
• Active Ingredient Strength: 25 mg/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 54799-503-15

15 mL in 1 BOTTLE, PLASTIC (54799-503-15)

• Marketing Start Date: 1989-10-02
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 54799-503-15 [54799050315]

GONIOSOFT LIQUID

• Marketing Category: unapproved drug other
• Product Type: HUMAN OTC DRUG
• Billing Unit: ML
• Marketing Start Date: 1989-10-02

Drug Details

Active Ingredients

Ingredient	Strength
HYPROMELLOSES	25 mg/mL

OpenFDA Data

• SPL SET ID: b9885de2-bd4c-c5c8-7ce3-c3f1669e74ea
• Manufacturer:
  • OCuSOFT, Inc.
• UNII:
  • 3NXW29V3WO
• RxNorm Concept Unique ID - RxCUI:
  • 206638
  • 310934
• UPC Code:
  • 0354799503151