Lansoprazole
- Product NDC
- 68071-5119
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA205868
- Marketing category
- ANDA
- Substance
- LANSOPRAZOLE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 68071-5119-3 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-5119-3) | 2019-12-20 | | No | Historical |
| 68071-5119-4 | 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-5119-4) | 2019-12-20 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Lansoprazole | NuCare Pharmaceuticals,Inc. | 2024-06-20 | HUMAN PRESCRIPTION DRUG LABEL | 6 |