Lansoprazole
- Product NDC
- 37012-117
- 11-digit product format
- 370120117
- Labeler code
- 37012
- Product ID
- 37012-117_413c8cc0-cd34-47ca-8e8c-d940222cf6df
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Shopko Stores Operating Co., LLC
- Application
- ANDA202319
- Marketing category
- ANDA
- Marketing start
- 2013-06-05
- Marketing end
- 0000-00-00
- Substance
- LANSOPRAZOLE
- Active strength
- 15 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 37012-117-01 | 37012011701 | 1 BOTTLE in 1 CARTON (37012-117-01) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 1 bottle | 2013-06-13 | 0000-00-00 | No | No | Current |
| 37012-117-02 | 37012011702 | 2 BOTTLE in 1 CARTON (37012-117-02) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 2 bottle | 2013-06-05 | 0000-00-00 | No | No | Current |
| 37012-117-03 | 37012011703 | 3 BOTTLE in 1 CARTON (37012-117-03) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 3 bottle | 2013-06-05 | 0000-00-00 | No | No | Current |