Lansoprazole 68001-0112
Product NDC
68001-0112- Manufacturer
- Bluepoint Laboratories
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 1, 2013
- Listing Expires
- December 31, 2026
- Application
- ANDA091269
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Lansoprazole | 30 mg/1 |
Drug Class
Proton Pump Inhibitor [EPC]Inhibition Gastric Acid Secretion [PE]Proton Pump Inhibitor [EPC]
Packaging Options(3)
500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-112-03)
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-112-04)
90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-112-05)