Lansoprazole
- Product NDC
- 69618-055
- 11-digit product format
- 696180055
- Labeler code
- 69618
- Product ID
- 69618-055_907bcf2d-0cc0-1d67-e053-2995a90a39d2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Reliable 1 Laboratories
- Application
- ANDA202194
- Marketing category
- ANDA
- Marketing start
- 2019-09-20
- 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
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 |
|---|
| 69618-055-42 | 69618005542 | 3 CAPSULE in 1 CARTON (69618-055-42) | 3 capsule | 2019-09-20 | 0000-00-00 | No | No | Current |