LANSOPRAZOLE
- Product NDC
- 72189-279
- 11-digit product format
- 721890279
- Labeler code
- 72189
- Product ID
- 72189-279_e0cd35eb-3938-659e-e053-2a95a90a6115
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LANSOPRAZOLE
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- DirectRx
- Application
- ANDA205868
- Marketing category
- ANDA
- Marketing start
- 2021-10-07
- Marketing end
- 0000-00-00
- Substance
- LANSOPRAZOLE
- Active strength
- 15 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 |
|---|
| 72189-279-60 | 72189027960 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-279-60) | 2021-10-07 | 0000-00-00 | No | No | Current |
| 72189-279-90 | 72189027990 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-279-90) | 2021-10-07 | 0000-00-00 | No | No | Current |