Lansoprazole
- Product NDC
- 71335-0043
- 11-digit product format
- 713350043
- Labeler code
- 71335
- Product ID
- 71335-0043_fc89a223-083b-4b70-9298-f07b52b66483
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA091269
- Marketing category
- ANDA
- Marketing start
- 2010-10-15
- 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 |
|---|
| 71335-0043-1 | 71335004301 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0043-1) | 2013-05-29 | 0000-00-00 | No | No | Current |
| 71335-0043-2 | 71335004302 | 15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0043-2) | 2013-05-29 | 0000-00-00 | No | No | Current |
| 71335-0043-3 | 71335004303 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0043-3) | 2013-05-29 | 0000-00-00 | No | No | Current |
| 71335-0043-4 | 71335004304 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0043-4) | 2013-05-29 | 0000-00-00 | No | No | Current |
| 71335-0043-5 | 71335004305 | 28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0043-5) | 2013-05-29 | 0000-00-00 | No | No | Current |