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ENTEX LQ
ENTEX LQ - 54868-6241-0 - (guaifenesin and phenylephrine hydrochloride)
Drug Information of ENTEX LQ
| Product NDC: | 54868-6241 |
| Proprietary Name: | ENTEX LQ |
| Non Proprietary Name: | guaifenesin and phenylephrine hydrochloride |
| Active Ingredient(s): | 100; 10 mg/5mL; mg/5mL & nbsp; guaifenesin and phenylephrine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ENTEX LQ
| Product NDC: | 54868-6241 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110401 |
Package Information of ENTEX LQ
| Package NDC: | 54868-6241-0 |
| Package Description: | 473 mL in 1 BOTTLE (54868-6241-0) |
NDC Information of ENTEX LQ
| NDC Code | 54868-6241-0 |
| Proprietary Name | ENTEX LQ |
| Package Description | 473 mL in 1 BOTTLE (54868-6241-0) |
| Product NDC | 54868-6241 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | guaifenesin and phenylephrine hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20110401 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 100; 10 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
