Lansoprazole
- Product NDC
- 62175-415
- 11-digit product format
- 621750415
- Labeler code
- 62175
- Product ID
- 62175-415_03c24721-9782-4090-9d8d-5517b3e7cbc9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE PELLETS
- Route
- ORAL
- Labeler
- Lannett Company, Inc.
- Application
- ANDA207156
- Marketing category
- ANDA
- Marketing start
- 2017-09-28
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 62175-415-32 | 62175041532 | 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (62175-415-32) | 2017-09-28 | 0000-00-00 | No | No | Current |
| 62175-415-37 | 62175041537 | 100 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (62175-415-37) | 2017-09-28 | 0000-00-00 | No | No | Current |
| 62175-415-41 | 62175041541 | 500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (62175-415-41) | 2017-09-28 | 0000-00-00 | No | No | Current |
| 62175-415-43 | 62175041543 | 1000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (62175-415-43) | 2017-09-28 | 0000-00-00 | No | No | Current |
| 62175-415-46 | 62175041546 | 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (62175-415-46) | 2017-09-28 | 0000-00-00 | No | No | Current |