Lansoprazole
- Product NDC
- 30142-019
- 11-digit product format
- 301420019
- Labeler code
- 30142
- Product ID
- 30142-019_86739cdf-7708-45ed-85fc-ee7ff87e7a52
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- The Kroger Co.
- Application
- ANDA202727
- Marketing category
- ANDA
- Marketing start
- 2012-09-01
- Marketing end
- 2019-12-31
- Substance
- LANSOPRAZOLE
- Active strength
- 15 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record