lansoprazole
- Product NDC
- 68788-7385
- 11-digit product format
- 687887385
- Labeler code
- 68788
- Product ID
- 68788-7385_5f194607-1ac0-48cb-b2bc-8bf9357726d9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE PELLETS
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA202366
- Marketing category
- ANDA
- Marketing start
- 2016-09-07
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- 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 |
|---|
| 68788-7385-1 | 68788738501 | 14 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-7385-1) | 2016-09-07 | 0000-00-00 | No | No | Current |
| 68788-7385-3 | 68788738503 | 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-7385-3) | 2016-09-07 | 0000-00-00 | No | No | Current |
| 68788-7385-6 | 68788738506 | 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-7385-6) | 2016-09-07 | 0000-00-00 | No | No | Current |
| 68788-7385-8 | 68788738508 | 120 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-7385-8) | 2016-09-07 | 0000-00-00 | No | No | Current |
| 68788-7385-9 | 68788738509 | 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-7385-9) | 2016-09-07 | 0000-00-00 | No | No | Current |