| NDC Code | 51655-548-26 |
|---|
| Package Description | 90 TABLET in 1 BOTTLE, PLASTIC (51655-548-26) |
|---|
| Product NDC | 51655-548 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Dicyclomine Hydrochloride |
|---|
| Non-Proprietary Name | Dicyclomine Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20230612 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA216736 |
|---|
| Manufacturer | Northwind Pharmaceuticals, LLC |
|---|
| Substance Name | DICYCLOMINE HYDROCHLORIDE |
|---|
| Strength | 20 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Anticholinergic [EPC], Cholinergic Antagonists [MoA] |
|---|