Lansoprazole
- Product NDC
- 0536-1324
- 11-digit product format
- 005361324
- Labeler code
- 0536
- Product ID
- 0536-1324_24a00d59-7f9b-a2bc-e454-d049e555756f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Rugby Laboratories
- Application
- ANDA202194
- Marketing category
- ANDA
- Marketing start
- 2020-11-12
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0536-1324-13 | 00536132413 | 3 BOTTLE in 1 CARTON (0536-1324-13) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 3 bottle | 2020-11-12 | 0000-00-00 | No | No | Current |
| 0536-1324-88 | 00536132488 | 1 BOTTLE in 1 CARTON (0536-1324-88) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 1 bottle | 2020-11-12 | 0000-00-00 | No | No | Current |