| NDC Code | 51660-071-36 |
|---|
| Package Description | 2 BLISTER PACK in 1 CARTON (51660-071-36) > 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
|---|
| Product NDC | 51660-071 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Guaifenesin And Pseudoephedrine Hydrochloride |
|---|
| Non-Proprietary Name | Guaifenesin And Pseudoephedrine Hydrochloride |
|---|
| Dosage Form | TABLET, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20171115 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA021585 |
|---|
| Manufacturer | OHM LABORATORIES INC |
|---|
| Substance Name | GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE |
|---|
| Strength | 600; 60 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Adrenergic alpha-Agonists [MoA], alpha-Adrenergic Agonist [EPC] |
|---|