Lansoprazole
- Product NDC
- 0591-2448
- 11-digit product format
- 005912448
- Labeler code
- 0591
- Product ID
- 0591-2448_0b480665-192f-49e3-87f3-38653d38ae68
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Actavis Pharma, Inc.
- Application
- ANDA203306
- Marketing category
- ANDA
- Marketing start
- 2016-01-13
- Marketing end
- 2019-07-31
- Substance
- LANSOPRAZOLE
- Active strength
- 15 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record