Lansoprazole
- Product NDC
- 68016-756
- 11-digit product format
- 680160756
- Labeler code
- 68016
- Product ID
- 68016-756_48647bc0-a548-4a11-88e8-b1841c739dd4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Chain Drug Consortium, LLC
- Application
- ANDA203306
- Marketing category
- ANDA
- Marketing start
- 2017-01-23
- Marketing end
- 2021-03-31
- Substance
- LANSOPRAZOLE
- Active strength
- 15 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68016-756-42 | 68016075642 | 3 BOTTLE in 1 CARTON (68016-756-42) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 3 bottle | 2017-01-23 | 2021-03-31 | No | No | Current |