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VANACOF
VANACOF - 58809-624-04 - (Chlophedianol Hydrochloride, Guaifenesin, Phenylephrine Hydrochloride)
Drug Information of VANACOF
| Product NDC: | 58809-624 |
| Proprietary Name: | VANACOF |
| Non Proprietary Name: | Chlophedianol Hydrochloride, Guaifenesin, Phenylephrine Hydrochloride |
| Active Ingredient(s): | 25; 200; 10 mg/15mL; mg/15mL; mg/15mL & nbsp; Chlophedianol Hydrochloride, Guaifenesin, Phenylephrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of VANACOF
| Product NDC: | 58809-624 |
| Labeler Name: | GM Pharmaceuticals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120929 |
Package Information of VANACOF
| Package NDC: | 58809-624-04 |
| Package Description: | 118 mL in 1 BOTTLE (58809-624-04) |
NDC Information of VANACOF
| NDC Code | 58809-624-04 |
| Proprietary Name | VANACOF |
| Package Description | 118 mL in 1 BOTTLE (58809-624-04) |
| Product NDC | 58809-624 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Chlophedianol Hydrochloride, Guaifenesin, Phenylephrine Hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20120929 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | GM Pharmaceuticals, Inc. |
| Substance Name | CHLOPHEDIANOL HYDROCHLORIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 25; 200; 10 |
| Strength Unit | mg/15mL; mg/15mL; mg/15mL |
| Pharmaceutical Classes |
