| NDC Code | 65197-204-42 |
|---|
| Package Description | 1 BOTTLE in 1 BOX (65197-204-42) / 42 TABLET, CHEWABLE in 1 BOTTLE |
|---|
| Product NDC | 65197-204 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Emetrol Chewables |
|---|
| Non-Proprietary Name | Sodium Citrate Dihydrate |
|---|
| Dosage Form | TABLET, CHEWABLE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20220315 |
|---|
| Marketing Category Name | UNAPPROVED DRUG OTHER |
|---|
| Manufacturer | WellSpring Pharmaceutical Corporation |
|---|
| Substance Name | TRISODIUM CITRATE DIHYDRATE |
|---|
| Strength | 230 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Acidifying Activity [MoA], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE] |
|---|