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GenTeal
GenTeal - 0078-0517-24 - (hypromellose)
Drug Information of GenTeal
| Product NDC: | 0078-0517 |
| Proprietary Name: | GenTeal |
| Non Proprietary Name: | hypromellose |
| Active Ingredient(s): | .002 L/L & nbsp; hypromellose |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of GenTeal
| Product NDC: | 0078-0517 |
| Labeler Name: | Novartis Pharmaceutical Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090914 |
Package Information of GenTeal
| Package NDC: | 0078-0517-24 |
| Package Description: | .015 L in 1 BOTTLE, DROPPER (0078-0517-24) |
NDC Information of GenTeal
| NDC Code | 0078-0517-24 |
| Proprietary Name | GenTeal |
| Package Description | .015 L in 1 BOTTLE, DROPPER (0078-0517-24) |
| Product NDC | 0078-0517 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | hypromellose |
| Dosage Form Name | LIQUID |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20090914 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Novartis Pharmaceutical Corporation |
| Substance Name | HYPROMELLOSE 2910 (4000 MPA.S) |
| Strength Number | .002 |
| Strength Unit | L/L |
| Pharmaceutical Classes |
