Berkley and Jensen Lansoprazole
- Product NDC
- 68391-117
- 11-digit product format
- 683910117
- Labeler code
- 68391
- Product ID
- 68391-117_db94410d-dbc3-4ed3-a44b-d46bcadad19a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- BJWC
- Application
- ANDA202319
- Marketing category
- ANDA
- Marketing start
- 2012-05-22
- 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 |
|---|
| 68391-117-03 | 68391011703 | 3 BOTTLE in 1 PACKAGE (68391-117-03) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 3 bottle | 2012-05-22 | 0000-00-00 | No | No | Current |