lansoprazole
- Product NDC
- 37808-117
- 11-digit product format
- 378080117
- Labeler code
- 37808
- Product ID
- 37808-117_e2ce818f-9259-41d0-8add-0bdbebcc60cc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- H E B
- Application
- ANDA202319
- Marketing category
- ANDA
- Marketing start
- 2012-05-18
- 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