Lansoprazole
- Product NDC
- 43598-883
- 11-digit product format
- 435980883
- Labeler code
- 43598
- Product ID
- 43598-883_dfa3d7c0-5421-de39-1e27-efd16a19fdc0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Dr. Reddy's Laboratories Inc.
- Application
- ANDA202194
- Marketing category
- ANDA
- Marketing start
- 2019-08-01
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43598-883 | LANSOPRAZOLE CAPSULE, DELAYED RELEASE [DR. REDDY'S LABORATORIES INC.] | 2 | Legacy NDC | 20231103_4b29b41e-2ec9-c7ce-24ad-acd459505cef.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43598-883-42 | 43598088342 | 3 BOTTLE in 1 CARTON (43598-883-42) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 3 bottle | 2019-08-01 | 0000-00-00 | No | No | Current |
| 43598-883-52 | 43598088352 | 1 BOTTLE in 1 CARTON (43598-883-52) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 1 bottle | 2019-08-01 | 0000-00-00 | No | No | Current |