Lansoprazole
- Product NDC
- 59726-019
- 11-digit product format
- 597260019
- Labeler code
- 59726
- Product ID
- 59726-019_e2d01781-5cfd-4fcb-b7fb-74961492c513
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- P & L Development, LLC
- Application
- ANDA202727
- Marketing category
- ANDA
- Marketing start
- 2013-01-15
- Marketing end
- 2020-12-31
- Substance
- LANSOPRAZOLE
- Active strength
- 15 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record