Trazodone
- Product NDC
- 51655-634
- 11-digit product format
- 516550634
- Labeler code
- 51655
- Product ID
- 51655-634_c9868405-01d9-5b53-e053-2995a90ac613
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trazodone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Northwind Pharmaceuticals, LLC
- Application
- ANDA071523
- Marketing category
- ANDA
- Marketing start
- 2014-12-01
- Marketing end
- 0000-00-00
- Substance
- TRAZODONE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC]
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51655-634-52 | 51655063452 | 30 TABLET in 1 BOTTLE, DISPENSING (51655-634-52) | 30 tablet | 2014-12-01 | 0000-00-00 | No | No | Current |