Lansoprazole
- Product NDC
- 16571-742
- 11-digit product format
- 165710742
- Labeler code
- 16571
- Product ID
- 16571-742_b8512fb0-87c2-45ae-b0db-189e467be449
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Rising Pharma Holdings, Inc.
- Application
- ANDA203306
- Marketing category
- ANDA
- Marketing start
- 2021-05-28
- Marketing end
- 0000-00-00
- Substance
- LANSOPRAZOLE
- Active strength
- 15 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 16571-742 | LANSOPRAZOLE CAPSULE, DELAYED RELEASE [RISING PHARMA HOLDINGS, INC.] | 1 | Legacy NDC | 20210529_b8512fb0-87c2-45ae-b0db-189e467be449.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16571-742-42 | 16571074242 | 3 BOTTLE in 1 CARTON (16571-742-42) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 3 bottle | 2021-05-28 | 0000-00-00 | No | No | Current |