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] |