Product NDC: | 49668-001 |
Proprietary Name: | Carboxymethylcellulose sodium |
Non Proprietary Name: | Carboxymethylcellulose sodium |
Active Ingredient(s): | 5 mg/mL & nbsp; Carboxymethylcellulose sodium |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49668-001 |
Labeler Name: | PROMED EXPORTS PRIVATE LIMITED |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part349 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20091001 |
Package NDC: | 49668-001-01 |
Package Description: | 30 VIAL, SINGLE-DOSE in 1 CONTAINER (49668-001-01) > .4 mL in 1 VIAL, SINGLE-DOSE |
NDC Code | 49668-001-01 |
Proprietary Name | Carboxymethylcellulose sodium |
Package Description | 30 VIAL, SINGLE-DOSE in 1 CONTAINER (49668-001-01) > .4 mL in 1 VIAL, SINGLE-DOSE |
Product NDC | 49668-001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Carboxymethylcellulose sodium |
Dosage Form Name | SOLUTION |
Route Name | OPHTHALMIC |
Start Marketing Date | 20091001 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | PROMED EXPORTS PRIVATE LIMITED |
Substance Name | CARBOXYMETHYLCELLULOSE SODIUM |
Strength Number | 5 |
Strength Unit | mg/mL |
Pharmaceutical Classes |