Varenicline Tartrate 71921-0309
Product NDC
71921-0309- Manufacturer
- Florida Pharmaceutical Products, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 1, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA219106
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Varenicline Tartrate | 1 mg/1 |
Drug Class
Cholinergic Agonists [MoA]Cholinergic Receptor Agonist [EPC]Partial Cholinergic Nicotinic Agonist [EPC]
Packaging Options(1)
56 TABLET, FILM COATED in 1 BOTTLE (71921-309-56)