smart sense lansoprazole
- Product NDC
- 49738-401
- 11-digit product format
- 497380401
- Labeler code
- 49738
- Product ID
- 49738-401_324f04e6-1a06-4d33-a4d5-a84f54af1912
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Kmart Corporation
- Application
- ANDA202319
- Marketing category
- ANDA
- Marketing start
- 2015-12-28
- 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