Trazodone Hydrochloride
- Product NDC
- 0615-2578
- 11-digit product format
- 006152578
- Labeler code
- 0615
- Product ID
- 0615-2578_0890fb8e-e2b6-47b1-93c1-01311a5b426d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trazodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Application
- ANDA071523
- Marketing category
- ANDA
- Marketing start
- 2011-01-20
- Marketing end
- 2022-06-30
- Substance
- TRAZODONE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 0615-2578-05 | 00615257805 | 15 TABLET in 1 BLISTER PACK (0615-2578-05) | 15 tablet | 2011-01-20 | 2022-06-30 | No | No | Current |
| 0615-2578-39 | 00615257839 | 30 TABLET in 1 BLISTER PACK (0615-2578-39) | 30 tablet | 2011-01-20 | 2022-06-30 | No | No | Current |