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Gonak Hypromellose
Gonak Hypromellose - 17478-064-12 - (Hypromellose 2906 (4000 MPA.S) and Hypromellose 2906 (50 MPA.S))
Drug Information of Gonak Hypromellose
| Product NDC: | 17478-064 |
| Proprietary Name: | Gonak Hypromellose |
| Non Proprietary Name: | Hypromellose 2906 (4000 MPA.S) and Hypromellose 2906 (50 MPA.S) |
| Active Ingredient(s): | 25; 25 mg/mL; mg/mL & nbsp; Hypromellose 2906 (4000 MPA.S) and Hypromellose 2906 (50 MPA.S) |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Gonak Hypromellose
| Product NDC: | 17478-064 |
| Labeler Name: | Akorn, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19970101 |
Package Information of Gonak Hypromellose
| Package NDC: | 17478-064-12 |
| Package Description: | 1 VIAL in 1 CARTON (17478-064-12) > 15 mL in 1 VIAL |
NDC Information of Gonak Hypromellose
| NDC Code | 17478-064-12 |
| Proprietary Name | Gonak Hypromellose |
| Package Description | 1 VIAL in 1 CARTON (17478-064-12) > 15 mL in 1 VIAL |
| Product NDC | 17478-064 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hypromellose 2906 (4000 MPA.S) and Hypromellose 2906 (50 MPA.S) |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19970101 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Akorn, Inc. |
| Substance Name | HYPROMELLOSE 2906 (4000 MPA.S); HYPROMELLOSE 2906 (50 MPA.S) |
| Strength Number | 25; 25 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |
