| NDC Code | 53808-0234-1 |
|---|
| Package Description | 30 TABLET in 1 BLISTER PACK (53808-0234-1) |
|---|
| Product NDC | 53808-0234 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Dicyclomine Hydrochloride |
|---|
| Non-Proprietary Name | Dicyclomine Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20090701 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA085223 |
|---|
| Manufacturer | State of Florida DOH Central Pharmacy |
|---|
| Substance Name | DICYCLOMINE HYDROCHLORIDE |
|---|
| Strength | 20 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA] |
|---|