lansoprazole
- Product NDC
- 68071-3019
- 11-digit product format
- 680713019
- Labeler code
- 68071
- Product ID
- 68071-3019_bb12a06b-008b-3cef-e053-2995a90a1ca1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE PELLETS
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA202366
- Marketing category
- ANDA
- Marketing start
- 2013-08-23
- Marketing end
- 0000-00-00
- Substance
- LANSOPRAZOLE
- Active strength
- 30 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-3019-3 | 68071301903 | 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68071-3019-3) | 2017-03-03 | 0000-00-00 | No | No | Current |
| 68071-3019-6 | 68071301906 | 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68071-3019-6) | 2017-03-03 | 0000-00-00 | No | No | Current |
| 68071-3019-7 | 68071301907 | 7 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68071-3019-7) | 2017-03-03 | 0000-00-00 | No | No | Current |