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NDC 63629-9863-01 Cevimeline Hydrochloride 30 mg/1 Details
Cevimeline Hydrochloride 30 mg/1
Cevimeline Hydrochloride is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is CEVIMELINE HYDROCHLORIDE.
MedlinePlus Drug Summary
Cevimeline is used to treat the symptoms of dry mouth in patients with Sjogren's syndrome (a condition that affects the immune system and causes dryness of certain parts of the body such as the eyes and mouth). Cevimeline is in a class of medications called cholinergic agonists. It works by increasing the amount of saliva in the mouth.
Related Packages: 63629-9863-01Last Updated: 04/28/2024
MedLinePlus Full Drug Details: Cevimeline
Product Information
| NDC | 63629-9863 |
|---|---|
| Product ID | 63629-9863_671bdcca-bd56-4802-8b20-53eb0b01e789 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Cevimeline Hydrochloride |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Cevimeline Hydrochloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | CAPSULE |
| Route | ORAL |
| Active Ingredient Strength | 30 |
| Active Ingredient Units | mg/1 |
| Substance Name | CEVIMELINE HYDROCHLORIDE |
| Labeler Name | Bryant Ranch Prepack |
| Pharmaceutical Class | Cholinergic Muscarinic Agonists [MoA], Cholinergic Receptor Agonist [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA203775 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 63629-9863-01 (63629986301)
| NDC Package Code | 63629-9863-1 |
|---|---|
| Billing NDC | 63629986301 |
| Package | 30 CAPSULE in 1 BOTTLE (63629-9863-1) |
| Marketing Start Date | 2023-10-27 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |