| NDC Code | 68071-1908-5 |
|---|
| Package Description | 15 TABLET in 1 BOTTLE (68071-1908-5) |
|---|
| Product NDC | 68071-1908 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Dicyclomine Hydrochloride |
|---|
| Non-Proprietary Name | Dicyclomine Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 19860730 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA085223 |
|---|
| Manufacturer | NuCare Pharmaceuticals, Inc. |
|---|
| Substance Name | DICYCLOMINE HYDROCHLORIDE |
|---|
| Strength | 20 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA] |
|---|