Lansoprazole
- Product NDC
- 0781-2148
- 11-digit product format
- 007812148
- Labeler code
- 0781
- Product ID
- 0781-2148_bd9e0dd5-2af9-419d-b6a9-7df460c8128a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Sandoz Inc
- Application
- ANDA090331
- Marketing category
- ANDA
- Marketing start
- 2010-04-23
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0781-2148-01 | 00781214801 | 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0781-2148-01) | 2010-04-23 | 0000-00-00 | No | No | Current |
| 0781-2148-10 | 00781214810 | 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0781-2148-10) | 2010-04-23 | 0000-00-00 | No | No | Current |
| 0781-2148-13 | 00781214813 | 100 CAPSULE, DELAYED RELEASE in 1 CARTON (0781-2148-13) | 2010-04-23 | 0000-00-00 | No | No | Current |
| 0781-2148-31 | 00781214831 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0781-2148-31) | 2010-04-23 | 0000-00-00 | No | No | Current |
| 0781-2148-71 | 00781214871 | 7 CAPSULE, DELAYED RELEASE in 1 CARTON (0781-2148-71) | 2010-04-23 | 0000-00-00 | No | No | Current |
| 0781-2148-92 | 00781214892 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0781-2148-92) | 2010-04-23 | 0000-00-00 | No | No | Current |