| Product NDC: | 17856-1161 |
| Proprietary Name: | dicyclomine hydrochloride |
| Non Proprietary Name: | dicyclomine hydrochloride |
| Active Ingredient(s): | 10 mg/5mL & nbsp; dicyclomine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 17856-1161 |
| Labeler Name: | Atlantic Biologicals Corps |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040169 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050623 |
| Package NDC: | 17856-1161-1 |
| Package Description: | 5 mL in 1 CUP (17856-1161-1) |
| NDC Code | 17856-1161-1 |
| Proprietary Name | dicyclomine hydrochloride |
| Package Description | 5 mL in 1 CUP (17856-1161-1) |
| Product NDC | 17856-1161 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | dicyclomine hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20050623 |
| Marketing Category Name | ANDA |
| Labeler Name | Atlantic Biologicals Corps |
| Substance Name | DICYCLOMINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA] |