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Bentyl
Bentyl - 58914-013-10 - (Dicyclomine hydrochloride)
Drug Information of Bentyl
| Product NDC: | 58914-013 |
| Proprietary Name: | Bentyl |
| Non Proprietary Name: | Dicyclomine hydrochloride |
| Active Ingredient(s): | 20.6 mg/1 & nbsp; Dicyclomine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Bentyl
| Product NDC: | 58914-013 |
| Labeler Name: | Aptalis Pharma US, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA007409 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19500511 |
Package Information of Bentyl
| Package NDC: | 58914-013-10 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (58914-013-10) |
NDC Information of Bentyl
| NDC Code | 58914-013-10 |
| Proprietary Name | Bentyl |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (58914-013-10) |
| Product NDC | 58914-013 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Dicyclomine hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19500511 |
| Marketing Category Name | NDA |
| Labeler Name | Aptalis Pharma US, Inc. |
| Substance Name | DICYCLOMINE HYDROCHLORIDE |
| Strength Number | 20.6 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA] |
