Basic Care Lansoprazole
- Product NDC
- 0113-7003
- 11-digit product format
- 001137003
- Labeler code
- 0113
- Product ID
- 0113-7003_41207e47-b4d7-411d-9ba9-ed3c12849bf1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- L. Perrigo Company
- Application
- ANDA202319
- Marketing category
- ANDA
- Marketing start
- 2017-09-03
- 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 table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0113-7003-03 | 00113700303 | 3 BOTTLE in 1 CARTON (0113-7003-03) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0113-7003-01) | 3 bottle | 2017-09-03 | 0000-00-00 | No | No | Current |