Home
>
National Drug Code (NDC)
>
Cevimeline Hydrochloride
Cevimeline Hydrochloride - 0054-0334-25 - (Cevimeline Hydrochloride)
Drug Information of Cevimeline Hydrochloride
| Product NDC: | 0054-0334 |
| Proprietary Name: | Cevimeline Hydrochloride |
| Non Proprietary Name: | Cevimeline Hydrochloride |
| Active Ingredient(s): | 30 mg/1 & nbsp; Cevimeline Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cevimeline Hydrochloride
| Product NDC: | 0054-0334 |
| Labeler Name: | Roxane Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091591 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130708 |
Package Information of Cevimeline Hydrochloride
| Package NDC: | 0054-0334-25 |
| Package Description: | 100 CAPSULE in 1 BOTTLE (0054-0334-25) |
NDC Information of Cevimeline Hydrochloride
| NDC Code | 0054-0334-25 |
| Proprietary Name | Cevimeline Hydrochloride |
| Package Description | 100 CAPSULE in 1 BOTTLE (0054-0334-25) |
| Product NDC | 0054-0334 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cevimeline Hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20130708 |
| Marketing Category Name | ANDA |
| Labeler Name | Roxane Laboratories, Inc. |
| Substance Name | CEVIMELINE HYDROCHLORIDE |
| Strength Number | 30 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cholinergic Muscarinic Agonists [MoA],Cholinergic Receptor Agonist [EPC] |
