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CARBATUSS
CARBATUSS - 58809-536-01 - (Carbetapentane Citrate, Phenylephrine Hydrochloride, Guaifenesin)
Drug Information of CARBATUSS
| Product NDC: | 58809-536 |
| Proprietary Name: | CARBATUSS |
| Non Proprietary Name: | Carbetapentane Citrate, Phenylephrine Hydrochloride, Guaifenesin |
| Active Ingredient(s): | 20; 100; 10 mg/5mL; mg/5mL; mg/5mL & nbsp; Carbetapentane Citrate, Phenylephrine Hydrochloride, Guaifenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CARBATUSS
| Product NDC: | 58809-536 |
| Labeler Name: | GM Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20001101 |
Package Information of CARBATUSS
| Package NDC: | 58809-536-01 |
| Package Description: | 473 mL in 1 BOTTLE (58809-536-01) |
NDC Information of CARBATUSS
| NDC Code | 58809-536-01 |
| Proprietary Name | CARBATUSS |
| Package Description | 473 mL in 1 BOTTLE (58809-536-01) |
| Product NDC | 58809-536 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Carbetapentane Citrate, Phenylephrine Hydrochloride, Guaifenesin |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20001101 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | GM Pharmaceuticals, Inc. |
| Substance Name | CARBETAPENTANE CITRATE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 20; 100; 10 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
