TRAZODONE HYDROCHLORIDE
- Product NDC
- 71335-3023
- 11-digit product format
- 713353023
- Labeler code
- 71335
- Product ID
- 71335-3023_fbba9e2a-10e3-4cc7-b46f-a2ac76420ff6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- TRAZODONE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA204852
- Marketing category
- ANDA
- Marketing start
- 2015-09-15
- Substance
- TRAZODONE HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- TRAZODONE HYDROCHLORIDE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TRAZODONE HYDROCHLORIDE | 100 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6E8ZO8LRNM |
| Rxcui | 856373 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-3023-1 | TRAZODONE HYDROCHLORIDE | 500 in 1 BOTTLE | TABLET | 500 | | 100 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-3023-1 | 71335302301 | 500 TABLET in 1 BOTTLE (71335-3023-1) | 500 tablet | 2025-12-04 | No | No | Historical |