Trazodone Hydrochloride
- Product NDC
- 53489-517
- 11-digit product format
- 534890517
- Labeler code
- 53489
- Product ID
- 53489-517_a4387b4a-d4d2-48b6-bd6d-e22b69547263
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trazodone Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Application
- ANDA073137
- Marketing category
- ANDA
- Marketing start
- 1993-03-24
- Marketing end
- 0000-00-00
- Substance
- TRAZODONE HYDROCHLORIDE
- Active strength
- 150 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 53489-517-01 | 53489051701 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-517-01) | 1993-03-24 | 0000-00-00 | No | No | Current |
| 53489-517-07 | 53489051707 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-517-07) | 1993-03-24 | 0000-00-00 | No | No | Current |