Lansoprazole
- Product NDC
- 68788-9281
- 11-digit product format
- 687889281
- Labeler code
- 68788
- Product ID
- 68788-9281_bdcdc078-851a-48f7-a55d-5e87f85246d5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA091269
- Marketing category
- ANDA
- Marketing start
- 2010-10-15
- Marketing end
- 0000-00-00
- Substance
- LANSOPRAZOLE
- Active strength
- 30 mg/1
- Pharmacologic classes
- Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Inhibition Gastric Acid Secretion [PE]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-9281-1 | 68788928101 | 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-9281-1) | 2010-10-15 | 0000-00-00 | No | No | Current |
| 68788-9281-3 | 68788928103 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-9281-3) | 2010-10-15 | 0000-00-00 | No | No | Current |
| 68788-9281-6 | 68788928106 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-9281-6) | 2010-10-15 | 0000-00-00 | No | No | Current |