NDC Code | 31722-079-10 |
Package Description | 1000 TABLET in 1 BOTTLE (31722-079-10) |
Product NDC | 31722-079 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Dicyclomine Hydrochloride |
Non-Proprietary Name | Dicyclomine Hydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20240507 |
Marketing Category Name | ANDA |
Application Number | ANDA217566 |
Manufacturer | Camber Pharmaceuticals, Inc. |
Substance Name | DICYCLOMINE HYDROCHLORIDE |
Strength | 20 |
Strength Unit | mg/1 |
Pharmacy Classes | Anticholinergic [EPC], Cholinergic Antagonists [MoA] |