Lansoprazole
- Product NDC
- 63868-008
- 11-digit product format
- 638680008
- Labeler code
- 63868
- Product ID
- 63868-008_c9ed5714-e519-4148-b48f-708ffc0d86fc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- QUALITY CHOICE (Chain Drug Marketing Association)
- Application
- ANDA202727
- Marketing category
- ANDA
- Marketing start
- 2013-04-30
- Marketing end
- 2019-12-30
- Substance
- LANSOPRAZOLE
- Active strength
- 15 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record