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VANACOF
VANACOF - 58809-907-01 - (Chlophedianol Hydrochloride, Guaifenesin, and Pseudoephedrine Hydrochloride)
Drug Information of VANACOF
| Product NDC: | 58809-907 |
| Proprietary Name: | VANACOF |
| Non Proprietary Name: | Chlophedianol Hydrochloride, Guaifenesin, and Pseudoephedrine Hydrochloride |
| Active Ingredient(s): | 12.5; 100; 30 mg/5mL; mg/5mL; mg/5mL & nbsp; Chlophedianol Hydrochloride, Guaifenesin, and Pseudoephedrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of VANACOF
| Product NDC: | 58809-907 |
| Labeler Name: | GM Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20080423 |
Package Information of VANACOF
| Package NDC: | 58809-907-01 |
| Package Description: | 473 mL in 1 BOTTLE (58809-907-01) |
NDC Information of VANACOF
| NDC Code | 58809-907-01 |
| Proprietary Name | VANACOF |
| Package Description | 473 mL in 1 BOTTLE (58809-907-01) |
| Product NDC | 58809-907 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Chlophedianol Hydrochloride, Guaifenesin, and Pseudoephedrine Hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20080423 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | GM Pharmaceuticals |
| Substance Name | CHLOPHEDIANOL HYDROCHLORIDE; GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 12.5; 100; 30 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
