| NDC Code | 70934-182-30 |
|---|
| Package Description | 30 TABLET in 1 BOTTLE, PLASTIC (70934-182-30) |
|---|
| Product NDC | 70934-182 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Dicyclomine Hydrochloride |
|---|
| Non-Proprietary Name | Dicyclomine Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20191205 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA040230 |
|---|
| Manufacturer | Denton Pharma, Inc. DBA Northwind Pharmaceuticals |
|---|
| Substance Name | DICYCLOMINE HYDROCHLORIDE |
|---|
| Strength | 20 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Anticholinergic [EPC], Cholinergic Antagonists [MoA] |
|---|