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Dicyclomine
Dicyclomine - 21695-218-30 - (Dicyclomine)
Drug Information of Dicyclomine
| Product NDC: | 21695-218 |
| Proprietary Name: | Dicyclomine |
| Non Proprietary Name: | Dicyclomine |
| Active Ingredient(s): | 10 mg/1 & nbsp; Dicyclomine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dicyclomine
| Product NDC: | 21695-218 |
| Labeler Name: | Rebel Distributors Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040204 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19970228 |
Package Information of Dicyclomine
| Package NDC: | 21695-218-30 |
| Package Description: | 30 CAPSULE in 1 BOTTLE, PLASTIC (21695-218-30) |
NDC Information of Dicyclomine
| NDC Code | 21695-218-30 |
| Proprietary Name | Dicyclomine |
| Package Description | 30 CAPSULE in 1 BOTTLE, PLASTIC (21695-218-30) |
| Product NDC | 21695-218 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Dicyclomine |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19970228 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp. |
| Substance Name | DICYCLOMINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA] |
