basic care lansoprazole
- Product NDC
- 0113-7116
- 11-digit product format
- 001137116
- Labeler code
- 0113
- Product ID
- 0113-7116_9b09acc9-656c-4764-a2d1-5606f1e10e4d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE
- Route
- ORAL
- Labeler
- L. Perrigo Company
- Application
- NDA208025
- Marketing category
- NDA
- Marketing start
- 2018-12-29
- Marketing end
- 0000-00-00
- Substance
- LANSOPRAZOLE
- Active strength
- 15 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 0113-7116-55 | 00113711655 | 3 CARTON in 1 CARTON (0113-7116-55) > 14 BLISTER PACK in 1 CARTON > 1 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK | 3 carton | 2018-12-29 | 0000-00-00 | No | No | Current |
| 0113-7116-74 | 00113711674 | 14 BLISTER PACK in 1 CARTON (0113-7116-74) > 1 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK | 14 blister pack | 2018-12-29 | 0000-00-00 | No | No | Current |