Lansoprazole
- Product NDC
- 68196-019
- 11-digit product format
- 681960019
- Labeler code
- 68196
- Product ID
- 68196-019_ec6eef48-b081-4fc2-8e00-e31206f4a42c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Sam's West, Inc
- Application
- ANDA202727
- Marketing category
- ANDA
- Marketing start
- 2013-03-30
- Marketing end
- 2019-08-31
- Substance
- LANSOPRAZOLE
- Active strength
- 15 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record