| NDC Code | 63868-143-10 |
|---|
| Package Description | 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (63868-143-10) |
|---|
| Product NDC | 63868-143 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Pseudoephedrine Hydrochloride |
|---|
| Non-Proprietary Name | Pseudoephedrine Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20060428 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA077442 |
|---|
| Manufacturer | Chain Drug Marketing Association Inc. |
|---|
| Substance Name | PSEUDOEPHEDRINE HYDROCHLORIDE |
|---|
| Strength | 120 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Adrenergic alpha-Agonists [MoA], alpha-Adrenergic Agonist [EPC] |
|---|