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LEADER DRY EYE RELIEF
LEADER DRY EYE RELIEF - 11716-9637-7 - (DEXTRAN 70)
Drug Information of LEADER DRY EYE RELIEF
| Product NDC: | 11716-9637 |
| Proprietary Name: | LEADER DRY EYE RELIEF |
| Non Proprietary Name: | DEXTRAN 70 |
| Active Ingredient(s): | .001; .003 mL/mL; mL/mL & nbsp; DEXTRAN 70 |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LEADER DRY EYE RELIEF
| Product NDC: | 11716-9637 |
| Labeler Name: | HANLIM PHARM. CO., LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100712 |
Package Information of LEADER DRY EYE RELIEF
| Package NDC: | 11716-9637-7 |
| Package Description: | 1 BOTTLE in 1 CARTON (11716-9637-7) > 15 mL in 1 BOTTLE |
NDC Information of LEADER DRY EYE RELIEF
| NDC Code | 11716-9637-7 |
| Proprietary Name | LEADER DRY EYE RELIEF |
| Package Description | 1 BOTTLE in 1 CARTON (11716-9637-7) > 15 mL in 1 BOTTLE |
| Product NDC | 11716-9637 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DEXTRAN 70 |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20100712 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | HANLIM PHARM. CO., LTD. |
| Substance Name | DEXTRAN 70; HYPROMELLOSE 2910 (4000 CPS) |
| Strength Number | .001; .003 |
| Strength Unit | mL/mL; mL/mL |
| Pharmaceutical Classes |
