Lansoprazole 68071-2734
Product NDC
68071-2734- Manufacturer
- Nucare Pharmaceuticals,inc.
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 18, 2020
- Listing Expires
- December 31, 2027
- Application
- ANDA203083
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Lansoprazole | 15 mg/1 |
Drug Class
Inhibition Gastric Acid Secretion [PE]Proton Pump Inhibitor [EPC]Proton Pump Inhibitors [MoA]
Packaging Options(2)
14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-2734-1)
60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-2734-6)