Lansoprazole
- Product NDC
- 62175-515
- 11-digit product format
- 621750515
- Labeler code
- 62175
- Product ID
- 62175-515_9d4be625-fedb-4b0a-bfcf-b8b513eeec8c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Lannett Company, Inc.
- Application
- ANDA207157
- Marketing category
- ANDA
- Marketing start
- 2017-09-29
- Marketing end
- 0000-00-00
- Substance
- LANSOPRAZOLE
- Active strength
- 15 mg/1
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 62175-515-12 | 62175051512 | 2 BOTTLE in 1 PACKAGE, COMBINATION (62175-515-12) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 2 bottle | 2017-09-29 | 0000-00-00 | No | No | Current |
| 62175-515-24 | 62175051524 | 1 BOTTLE in 1 CARTON (62175-515-24) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 1 bottle | 2017-09-29 | 0000-00-00 | No | No | Current |
| 62175-515-52 | 62175051552 | 3 BOTTLE in 1 PACKAGE, COMBINATION (62175-515-52) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 3 bottle | 2017-09-29 | 0000-00-00 | No | No | Current |