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Entex PAC
Entex PAC - 66992-285-34 - (Guaifenesin, Pseudoephedrine Hydrochloride, Dextromethorphan Hydrobromide)
Drug Information of Entex PAC
| Product NDC: | 66992-285 |
| Proprietary Name: | Entex PAC |
| Non Proprietary Name: | Guaifenesin, Pseudoephedrine Hydrochloride, Dextromethorphan Hydrobromide |
| Active Ingredient(s): | & nbsp; Guaifenesin, Pseudoephedrine Hydrochloride, Dextromethorphan Hydrobromide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Entex PAC
| Product NDC: | 66992-285 |
| Labeler Name: | WraSer Pharmaceuticals, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110830 |
Package Information of Entex PAC
| Package NDC: | 66992-285-34 |
| Package Description: | 1 KIT in 1 PACKAGE, COMBINATION (66992-285-34) * 30 TABLET in 1 BOTTLE (66992-281-30) * 118 mL in 1 BOTTLE (66992-290-04) |
NDC Information of Entex PAC
| NDC Code | 66992-285-34 |
| Proprietary Name | Entex PAC |
| Package Description | 1 KIT in 1 PACKAGE, COMBINATION (66992-285-34) * 30 TABLET in 1 BOTTLE (66992-281-30) * 118 mL in 1 BOTTLE (66992-290-04) |
| Product NDC | 66992-285 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin, Pseudoephedrine Hydrochloride, Dextromethorphan Hydrobromide |
| Dosage Form Name | KIT |
| Route Name | ORAL |
| Start Marketing Date | 20110830 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | WraSer Pharmaceuticals, LLC |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
