Lansoprazole
- Product NDC
- 68071-3633
- 11-digit product format
- 680713633
- Labeler code
- 68071
- Product ID
- 68071-3633_2abc8a40-b8ab-5177-e063-6394a90a70de
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA205868
- Marketing category
- ANDA
- Marketing start
- 2018-06-04
- Substance
- LANSOPRAZOLE
- Active strength
- 15 mg/1
- Pharmacologic classes
- Inhibition Gastric Acid Secretion [PE], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 0K5C5T2QPG | LANSOPRAZOLE | 103577-45-3 | LANSOPRAZOLE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 68071-3633-3 | 68071363303 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3633-3) | 2024-07-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Lansoprazole | NuCare Pharmaceuticals,Inc. | 2025-01-02 | HUMAN PRESCRIPTION DRUG LABEL | 2 |