| Product NDC: | 15370-033 |
| Proprietary Name: | NU-COPD |
| Non Proprietary Name: | Guaifenesin and Phenylephrine Hydrochloride |
| Active Ingredient(s): | 400; 10 mg/1; mg/1 & nbsp; Guaifenesin and Phenylephrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 15370-033 |
| Labeler Name: | CARWIN ASSOCIATES, INC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120415 |
| Package NDC: | 15370-033-05 |
| Package Description: | 1 BLISTER PACK in 1 BOX (15370-033-05) > 5 TABLET in 1 BLISTER PACK |
| NDC Code | 15370-033-05 |
| Proprietary Name | NU-COPD |
| Package Description | 1 BLISTER PACK in 1 BOX (15370-033-05) > 5 TABLET in 1 BLISTER PACK |
| Product NDC | 15370-033 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin and Phenylephrine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120415 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | CARWIN ASSOCIATES, INC |
| Substance Name | GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 400; 10 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |