Lansoprazole
- Product NDC
- 68788-7789
- 11-digit product format
- 687887789
- Labeler code
- 68788
- Product ID
- 68788-7789_9eb2aa06-282b-4f62-9c21-65cbd39bc98e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE PELLETS
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA207156
- Marketing category
- ANDA
- Marketing start
- 2020-10-21
- Marketing end
- 0000-00-00
- Substance
- LANSOPRAZOLE
- Active strength
- 15 mg/1
- Pharmacologic classes
- Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Inhibition Gastric Acid Secretion [PE]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 68788-7789-1 | 68788778901 | 100 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-7789-1) | 2020-10-21 | 0000-00-00 | No | No | Current |
| 68788-7789-3 | 68788778903 | 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-7789-3) | 2020-10-21 | 0000-00-00 | No | No | Current |
| 68788-7789-6 | 68788778906 | 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-7789-6) | 2020-10-21 | 0000-00-00 | No | No | Current |
| 68788-7789-8 | 68788778908 | 120 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-7789-8) | 2020-10-21 | 0000-00-00 | No | No | Current |
| 68788-7789-9 | 68788778909 | 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-7789-9) | 2020-10-21 | 0000-00-00 | No | No | Current |