LANSOPRAZOLE
- Product NDC
- 50090-2739
- 11-digit product format
- 500902739
- Labeler code
- 50090
- Product ID
- 50090-2739_74839039-091f-4367-b6ee-7b0fa0bbefbf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LANSOPRAZOLE
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA201921
- Marketing category
- ANDA
- Marketing start
- 2012-12-18
- 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
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record