Lansoprazole
- Product NDC
- 50090-5180
- 11-digit product format
- 500905180
- Labeler code
- 50090
- Product ID
- 50090-5180_ee55f98b-3781-4ac3-ad33-4e265b551603
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA207394
- Marketing category
- ANDA
- Marketing start
- 2019-01-20
- Substance
- LANSOPRAZOLE
- Active strength
- 30 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 |
|---|
| 50090-5180-0 | 50090518000 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-5180-0) | 2020-09-28 | No | No | Historical |
| 50090-5180-1 | 50090518001 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-5180-1) | 2020-09-28 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Lansoprazole | A-S Medication Solutions | 2023-06-22 | Human Prescription Drug Label | 7 |