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GONIOSOFT
GONIOSOFT - 54799-503-15 - (Hypromellose 2.5%)
Drug Information of GONIOSOFT
| Product NDC: | 54799-503 |
| Proprietary Name: | GONIOSOFT |
| Non Proprietary Name: | Hypromellose 2.5% |
| Active Ingredient(s): | 25 mg/mL & nbsp; Hypromellose 2.5% |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of GONIOSOFT
| Product NDC: | 54799-503 |
| Labeler Name: | OCuSOFT, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19891002 |
Package Information of GONIOSOFT
| Package NDC: | 54799-503-15 |
| Package Description: | 15 mL in 1 BOTTLE, PLASTIC (54799-503-15) |
NDC Information of GONIOSOFT
| NDC Code | 54799-503-15 |
| Proprietary Name | GONIOSOFT |
| Package Description | 15 mL in 1 BOTTLE, PLASTIC (54799-503-15) |
| Product NDC | 54799-503 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Hypromellose 2.5% |
| Dosage Form Name | LIQUID |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19891002 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | OCuSOFT, Inc. |
| Substance Name | HYPROMELLOSES |
| Strength Number | 25 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
