Lansoprazole
- Product NDC
- 71335-2957
- 11-digit product format
- 713352957
- Labeler code
- 71335
- Product ID
- 71335-2957_98b30e46-1539-4cd5-9205-059368298529
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA091269
- Marketing category
- ANDA
- Marketing start
- 2010-10-15
- 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 |
|---|
| 71335-2957-1 | 71335295701 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2957-1) | 2025-10-28 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Lansoprazole | Bryant Ranch Prepack | 2025-10-28 | HUMAN PRESCRIPTION DRUG LABEL | 100 |