Lansoprazole
- Product NDC
- 63868-429
- 11-digit product format
- 638680429
- Labeler code
- 63868
- Product ID
- 63868-429_236ccaaa-8eea-b6c0-575c-d3de258b751a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Chain Drug Marketing Association
- Application
- ANDA202194
- Marketing category
- ANDA
- Marketing start
- 2019-09-13
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63868-429 | LANSOPRAZOLE CAPSULE, DELAYED RELEASE [CHAIN DRUG MARKETING ASSOCIATION] | 2 | Legacy NDC | 20241203_5aaa28e5-bfb2-2c85-3996-19404354ed39.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63868-429-14 | 63868042914 | 1 BOTTLE in 1 CARTON (63868-429-14) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 1 bottle | 2019-09-13 | 0000-00-00 | No | No | Current |
| 63868-429-42 | 63868042942 | 3 BOTTLE in 1 CARTON (63868-429-42) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 3 bottle | 2019-09-13 | 0000-00-00 | No | No | Current |