lansoprazole
- Product NDC
- 41250-391
- 11-digit product format
- 412500391
- Labeler code
- 41250
- Product ID
- 41250-391_9061499d-aba8-4500-abc0-22d915458cbc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Meijer Distribution Inc
- Application
- ANDA202319
- Marketing category
- ANDA
- Marketing start
- 2021-06-07
- 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 | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 41250-391-01 | 41250039101 | 1 BOTTLE in 1 CARTON (41250-391-01) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 1 bottle | 2021-06-07 | No | No | Historical |
| 41250-391-03 | 41250039103 | 3 BOTTLE in 1 CARTON (41250-391-03) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 3 bottle | 2021-06-07 | No | No | Historical |