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Dicyclomine
Dicyclomine - 63629-1299-1 - (Dicyclomine Hydrochloride)
Drug Information of Dicyclomine
| Product NDC: | 63629-1299 |
| Proprietary Name: | Dicyclomine |
| Non Proprietary Name: | Dicyclomine Hydrochloride |
| Active Ingredient(s): | 20 mg/1 & nbsp; Dicyclomine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dicyclomine
| Product NDC: | 63629-1299 |
| Labeler Name: | Bryant Ranch Prepack |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040161 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19961001 |
Package Information of Dicyclomine
| Package NDC: | 63629-1299-1 |
| Package Description: | 30 TABLET in 1 BOTTLE (63629-1299-1) |
NDC Information of Dicyclomine
| NDC Code | 63629-1299-1 |
| Proprietary Name | Dicyclomine |
| Package Description | 30 TABLET in 1 BOTTLE (63629-1299-1) |
| Product NDC | 63629-1299 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Dicyclomine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19961001 |
| Marketing Category Name | ANDA |
| Labeler Name | Bryant Ranch Prepack |
| Substance Name | DICYCLOMINE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA] |
