Lansoprazole
- Product NDC
- 71335-0660
- 11-digit product format
- 713350660
- Labeler code
- 71335
- Product ID
- 71335-0660_017ed3d2-e9c8-42a1-9ea2-0b6832a7bd9e
- 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
- 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 |
|---|
| 71335-0660-1 | 71335066001 | 56 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0660-1) | 2010-10-15 | 0000-00-00 | No | No | Current |
| 71335-0660-2 | 71335066002 | 28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0660-2) | 2010-10-15 | 0000-00-00 | No | No | Current |
| 71335-0660-3 | 71335066003 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0660-3) | 2010-10-15 | 0000-00-00 | No | No | Current |
| 71335-0660-4 | 71335066004 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0660-4) | 2010-10-15 | 0000-00-00 | No | No | Current |
| 71335-0660-5 | 71335066005 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0660-5) | 2010-10-15 | 0000-00-00 | No | No | Current |
| 71335-0660-6 | 71335066006 | 58 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0660-6) | 2010-10-15 | 0000-00-00 | No | No | Current |
| 71335-0660-7 | 71335066007 | 18 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0660-7) | 2010-10-15 | 0000-00-00 | No | No | Current |