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lubricating plus
lubricating plus - 0904-6329-51 - (carboxymethylcellulose sodium)
Drug Information of lubricating plus
| Product NDC: | 0904-6329 |
| Proprietary Name: | lubricating plus |
| Non Proprietary Name: | carboxymethylcellulose sodium |
| Active Ingredient(s): | .5 g/100mL & nbsp; carboxymethylcellulose sodium |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION, GEL FORMING / DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of lubricating plus
| Product NDC: | 0904-6329 |
| Labeler Name: | Major Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130509 |
Package Information of lubricating plus
| Package NDC: | 0904-6329-51 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (0904-6329-51) > 5 POUCH in 1 BLISTER PACK > .4 mL in 1 POUCH |
NDC Information of lubricating plus
| NDC Code | 0904-6329-51 |
| Proprietary Name | lubricating plus |
| Package Description | 10 BLISTER PACK in 1 CARTON (0904-6329-51) > 5 POUCH in 1 BLISTER PACK > .4 mL in 1 POUCH |
| Product NDC | 0904-6329 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | carboxymethylcellulose sodium |
| Dosage Form Name | SOLUTION, GEL FORMING / DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20130509 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Major Pharmaceuticals |
| Substance Name | CARBOXYMETHYLCELLULOSE SODIUM |
| Strength Number | .5 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes |
