lansoprazole
- Product NDC
- 71335-0105
- 11-digit product format
- 713350105
- Labeler code
- 71335
- Product ID
- 71335-0105_40dde670-b9ad-4f05-aa6f-aa1ff6cf1b9b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE PELLETS
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- 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
- 2021-12-31
- 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 |
|---|
| 71335-0105-1 | 71335010501 | 56 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0105-1) | 2013-08-23 | 0000-00-00 | No | No | Current |
| 71335-0105-2 | 71335010502 | 28 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0105-2) | 2013-08-23 | 0000-00-00 | No | No | Current |
| 71335-0105-3 | 71335010503 | 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0105-3) | 2013-08-23 | 0000-00-00 | No | No | Current |
| 71335-0105-4 | 71335010504 | 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0105-4) | 2013-08-23 | 0000-00-00 | No | No | Current |
| 71335-0105-5 | 71335010505 | 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0105-5) | 2013-08-23 | 0000-00-00 | No | No | Current |
| 71335-0105-6 | 71335010506 | 58 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0105-6) | 2013-08-23 | 0000-00-00 | No | No | Current |
| 71335-0105-7 | 71335010507 | 18 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0105-7) | 2013-08-23 | 0000-00-00 | No | No | Current |