lansoprazole
- Product NDC
- 50090-1945
- 11-digit product format
- 500901945
- Labeler code
- 50090
- Product ID
- 50090-1945_6d3dd6a6-b450-4286-be61-bc48e6988aff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE PELLETS
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA202366
- Marketing category
- ANDA
- Marketing start
- 2013-08-23
- Marketing end
- 0000-00-00
- Substance
- LANSOPRAZOLE
- Active strength
- 15 mg/1
- Pharmacologic classes
- Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Inhibition Gastric Acid Secretion [PE]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#