| Product NDC: | 63629-3341 |
| Proprietary Name: | dicyclomine hydrochloride |
| Non Proprietary Name: | dicyclomine hydrochloride |
| Active Ingredient(s): | 10 mg/1 & nbsp; dicyclomine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 63629-3341 |
| Labeler Name: | Bryant Ranch Prepack |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040204 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19970228 |
| Package NDC: | 63629-3341-2 |
| Package Description: | 90 CAPSULE in 1 BOTTLE (63629-3341-2) |
| NDC Code | 63629-3341-2 |
| Proprietary Name | dicyclomine hydrochloride |
| Package Description | 90 CAPSULE in 1 BOTTLE (63629-3341-2) |
| Product NDC | 63629-3341 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | dicyclomine hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19970228 |
| Marketing Category Name | ANDA |
| Labeler Name | Bryant Ranch Prepack |
| Substance Name | DICYCLOMINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA] |