Lansoprazole
- Product NDC
- 37808-448
- 11-digit product format
- 378080448
- Labeler code
- 37808
- Product ID
- 37808-448_c7379031-b622-41be-8afd-ac1f44ff4e33
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- HEB
- Application
- ANDA203306
- Marketing category
- ANDA
- Marketing start
- 2018-12-03
- Marketing end
- 2021-03-31
- Substance
- LANSOPRAZOLE
- Active strength
- 15 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 37808-448-14 | 37808044814 | 1 BOTTLE in 1 CARTON (37808-448-14) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 1 bottle | 2018-12-03 | 2021-03-31 | No | No | Current |
| 37808-448-42 | 37808044842 | 3 BOTTLE in 1 CARTON (37808-448-42) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 3 bottle | 2018-12-14 | 2021-03-31 | No | No | Current |