Trazodone Hydrochloride
- Product NDC
- 68071-3124
- 11-digit product format
- 680713124
- Labeler code
- 68071
- Product ID
- 68071-3124_af857f13-398d-45b3-e053-2995a90aebbd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trazodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA071524
- Marketing category
- ANDA
- Marketing start
- 1990-09-30
- Marketing end
- 0000-00-00
- Substance
- TRAZODONE HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 68071-3124-3 | 68071312403 | 30 TABLET in 1 BOTTLE (68071-3124-3) | 30 tablet | 1990-09-30 | 0000-00-00 | No | No | Current |
| 68071-3124-5 | 68071312405 | 45 TABLET in 1 BOTTLE (68071-3124-5) | 45 tablet | 1990-09-30 | 0000-00-00 | No | No | Current |
| 68071-3124-6 | 68071312406 | 60 TABLET in 1 BOTTLE (68071-3124-6) | 60 tablet | 1990-09-30 | 0000-00-00 | No | No | Current |
| 68071-3124-9 | 68071312409 | 90 TABLET in 1 BOTTLE (68071-3124-9) | 90 tablet | 1990-09-30 | 0000-00-00 | No | No | Current |