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Guaifenesin DAC
Guaifenesin DAC - 16571-301-16 - (Guaifenesin, Codeine Phosphate and Pseudoephedrine Hydrochloride)
Drug Information of Guaifenesin DAC
| Product NDC: | 16571-301 |
| Proprietary Name: | Guaifenesin DAC |
| Non Proprietary Name: | Guaifenesin, Codeine Phosphate and Pseudoephedrine Hydrochloride |
| Active Ingredient(s): | 10; 100; 30 mg/5mL; mg/5mL; mg/5mL & nbsp; Guaifenesin, Codeine Phosphate and Pseudoephedrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Guaifenesin DAC
| Product NDC: | 16571-301 |
| Labeler Name: | Pack Pharmaceuticals LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED OTHER |
| Start Marketing Date: | 20090928 |
Package Information of Guaifenesin DAC
| Package NDC: | 16571-301-16 |
| Package Description: | 473 mL in 1 BOTTLE (16571-301-16) |
NDC Information of Guaifenesin DAC
| NDC Code | 16571-301-16 |
| Proprietary Name | Guaifenesin DAC |
| Package Description | 473 mL in 1 BOTTLE (16571-301-16) |
| Product NDC | 16571-301 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin, Codeine Phosphate and Pseudoephedrine Hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20090928 |
| Marketing Category Name | UNAPPROVED OTHER |
| Labeler Name | Pack Pharmaceuticals LLC |
| Substance Name | CODEINE PHOSPHATE; GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 10; 100; 30 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
