LANSOPRAZOLE
- Product NDC
- 61919-890
- 11-digit product format
- 619190890
- Labeler code
- 61919
- Product ID
- 61919-890_86be80d9-deab-f4ce-e053-2991aa0aa74c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LANSOPRAZOLE
- Dosage form
- CAPSULE, DELAYED RELEASE PELLETS
- Route
- ORAL
- Labeler
- Direct RX
- Application
- ANDA202366
- Marketing category
- ANDA
- Marketing start
- 2014-01-01
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-890-30 | 61919089030 | 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (61919-890-30) | 2014-01-01 | 0000-00-00 | No | No | Current |