Cevimeline Hydrochloride 43386-0999
Product NDC
43386-0999- Manufacturer
- Lupin Pharmaceuticals,inc.
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 30, 2016
- Listing Expires
- December 31, 2026
- Application
- ANDA204746
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Cevimeline Hydrochloride | 30 mg/1 |
Drug Class
Cholinergic Muscarinic Agonists [MoA]Cholinergic Receptor Agonist [EPC]