Guaifenesin DAC - Guaifenesin, Codeine Phosphate and Pseudoephedrine Hydrochloride
Navigation: NDC > Supplier starting with: P > PACK PHARMACEUTICALS LLC| Field | Value |
|---|---|
| NDC Code: | 16571-301 |
| Proprietary Name: | Guaifenesin DAC |
| Suffix: | |
| Non-Proprietary Name: | Guaifenesin, Codeine Phosphate and Pseudoephedrine Hydrochloride |
| Dosage Form: | LIQUID |
| Method: | ORAL |
| Original Marketing Date: | 28-09-2009 |
| Category Name: | UNAPPROVED OTHER |
| Application Number: | |
| Labeler: | PACK PHARMACEUTICALS LLC |
| Substance Name: | CODEINE PHOSPHATE; GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Active Numerator Strength: | 10; 100; 30 |
| Active Ingredient Unit: | mg/5mL; mg/5mL; mg/5mL |
| Pharm Classes: | |
| DEA Schedule: | CV |