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nexafed
nexafed - 48964-112-24 - (pseudoephedrine HCL)
Drug Information of nexafed
| Product NDC: | 48964-112 |
| Proprietary Name: | nexafed |
| Non Proprietary Name: | pseudoephedrine HCL |
| Active Ingredient(s): | 30 mg/1 & nbsp; pseudoephedrine HCL |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of nexafed
| Product NDC: | 48964-112 |
| Labeler Name: | Acura Pharmaceuticals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121210 |
Package Information of nexafed
| Package NDC: | 48964-112-24 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (48964-112-24) > 12 TABLET in 1 BLISTER PACK |
NDC Information of nexafed
| NDC Code | 48964-112-24 |
| Proprietary Name | nexafed |
| Package Description | 2 BLISTER PACK in 1 CARTON (48964-112-24) > 12 TABLET in 1 BLISTER PACK |
| Product NDC | 48964-112 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | pseudoephedrine HCL |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20121210 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Acura Pharmaceuticals, Inc. |
| Substance Name | PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 30 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
