LANSOPRAZOLE
- Product NDC
- 72189-062
- 11-digit product format
- 721890062
- Labeler code
- 72189
- Product ID
- 72189-062_e9d2cf34-fe63-1398-e053-2995a90a11ff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LANSOPRAZOLE
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA091269
- Marketing category
- ANDA
- Marketing start
- 2019-11-20
- Marketing end
- 0000-00-00
- Substance
- LANSOPRAZOLE
- Active strength
- 30 mg/1
- Pharmacologic classes
- Inhibition Gastric Acid Secretion [PE], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 72189-062-30 | 72189006230 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-062-30) | 2019-11-20 | 0000-00-00 | No | No | Current |
| 72189-062-90 | 72189006290 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-062-90) | 2019-11-20 | 0000-00-00 | No | No | Current |