lansoprazole
- Product NDC
- 50268-465
- 11-digit product format
- 502680465
- Labeler code
- 50268
- Product ID
- 50268-465_ba4d38de-7ad7-d719-e053-2a95a90a042e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE PELLETS
- Route
- ORAL
- Labeler
- AvPAK
- Application
- ANDA202366
- Marketing category
- ANDA
- Marketing start
- 2016-07-14
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50268-465-15 | 50268046515 | 50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-465-15) > 1 CAPSULE, DELAYED RELEASE PELLETS in 1 BLISTER PACK (50268-465-11) | 50 blister pack | 2016-07-14 | 0000-00-00 | No | No | Current |