Home
>
National Drug Code (NDC)
>
DICYCLOMINE
DICYCLOMINE - 16590-324-72 - (DICYCLOMINE HYDROCHLORIDE)
Drug Information of DICYCLOMINE
| Product NDC: | 16590-324 |
| 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: | 16590-324 |
| Labeler Name: | STAT RX USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040161 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19961001 |
Package Information of DICYCLOMINE
| Package NDC: | 16590-324-72 |
| Package Description: | 120 TABLET in 1 BOTTLE, PLASTIC (16590-324-72) |
NDC Information of DICYCLOMINE
| NDC Code | 16590-324-72 |
| Proprietary Name | DICYCLOMINE |
| Package Description | 120 TABLET in 1 BOTTLE, PLASTIC (16590-324-72) |
| Product NDC | 16590-324 |
| 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 | STAT RX USA LLC |
| Substance Name | DICYCLOMINE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA] |
