| NDC Code | 68788-7811-2 |
|---|
| Package Description | 20 TABLET in 1 BOTTLE (68788-7811-2) |
|---|
| Product NDC | 68788-7811 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Dicyclomine Hydrochloride |
|---|
| Non-Proprietary Name | Dicyclomine Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20201103 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA040230 |
|---|
| Manufacturer | Preferred Pharmaceuticals Inc. |
|---|
| Substance Name | DICYCLOMINE HYDROCHLORIDE |
|---|
| Strength | 20 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Anticholinergic [EPC], Cholinergic Antagonists [MoA] |
|---|