Tekturna
- Product NDC
- 50090-2985
- 11-digit product format
- 500902985
- Labeler code
- 50090
- Product ID
- 50090-2985_9f44ea37-b3cc-4927-8f8a-1be8325b9519
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- aliskiren hemifumarate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- NDA021985
- Marketing category
- NDA
- Marketing start
- 2007-03-05
- Marketing end
- 0000-00-00
- Substance
- ALISKIREN HEMIFUMARATE
- Active strength
- 300 mg/1
- Pharmacologic classes
- Renin Inhibitor [EPC],Renin 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 |
|---|
| 50090-2985-0 | 50090298500 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-2985-0) | 2017-04-25 | 0000-00-00 | No | No | Current |