Lansoprazole
- Product NDC
- 71335-2078
- 11-digit product format
- 713352078
- Labeler code
- 71335
- Product ID
- 71335-2078_66bcfec6-d039-419f-a2d7-cb7e6e659cf1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA205868
- Marketing category
- ANDA
- Marketing start
- 2018-06-04
- 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 |
|---|
| 71335-2078-1 | 71335207801 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2078-1) | 2022-04-25 | 0000-00-00 | No | No | Current |
| 71335-2078-2 | 71335207802 | 15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2078-2) | 2022-04-25 | 0000-00-00 | No | No | Current |
| 71335-2078-3 | 71335207803 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2078-3) | 2022-04-25 | 0000-00-00 | No | No | Current |
| 71335-2078-4 | 71335207804 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2078-4) | 2022-04-25 | 0000-00-00 | No | No | Current |
| 71335-2078-5 | 71335207805 | 28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2078-5) | 2022-04-25 | 0000-00-00 | No | No | Current |