Dexilant
- Product NDC
- 50090-4374
- 11-digit product format
- 500904374
- Labeler code
- 50090
- Product ID
- 50090-4374_b5314019-ccda-448f-8681-1b2fb9db629d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dexlansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- NDA022287
- Marketing category
- NDA
- Marketing start
- 2010-04-12
- Marketing end
- 0000-00-00
- Substance
- DEXLANSOPRAZOLE
- Active strength
- 60 mg/1
- Pharmacologic classes
- Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4374-0 | 50090437400 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-4374-0) | 2019-06-20 | 0000-00-00 | No | No | Current |