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Dicyclomine
Dicyclomine - 68788-9935-3 - (dicyclomine hydrochloride)
Drug Information of Dicyclomine
| Product NDC: | 68788-9935 |
| Proprietary Name: | Dicyclomine |
| 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) |
Labeler Information of Dicyclomine
| Product NDC: | 68788-9935 |
| Labeler Name: | Preferred Pharmaceuticals, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040204 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120117 |
Package Information of Dicyclomine
| Package NDC: | 68788-9935-3 |
| Package Description: | 30 CAPSULE in 1 BOTTLE, PLASTIC (68788-9935-3) |
NDC Information of Dicyclomine
| NDC Code | 68788-9935-3 |
| Proprietary Name | Dicyclomine |
| Package Description | 30 CAPSULE in 1 BOTTLE, PLASTIC (68788-9935-3) |
| Product NDC | 68788-9935 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | dicyclomine hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20120117 |
| Marketing Category Name | ANDA |
| Labeler Name | Preferred Pharmaceuticals, Inc |
| Substance Name | DICYCLOMINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA] |
