Trazodone Hydrochloride
- Product NDC
- 70518-2180
- 11-digit product format
- 705182180
- Labeler code
- 70518
- Product ID
- 70518-2180_49db46f7-1ae9-7c94-e063-6294a90a94e3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trazodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA205253
- Marketing category
- ANDA
- Marketing start
- 2019-07-01
- Substance
- TRAZODONE HYDROCHLORIDE
- Active strength
- 150 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Trazodone Hydrochloride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TRAZODONE HYDROCHLORIDE | 150 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6E8ZO8LRNM |
| Rxcui | 856364 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-2180-0 | Trazodone Hydrochloride | 90 in 1 BOTTLE, PLASTIC | TABLET | 90 | | 8 |
| 70518-2180-1 | Trazodone Hydrochloride | 30 in 1 BLISTER PACK | TABLET | 30 | | 8 |
| 70518-2180-2 | Trazodone Hydrochloride | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | | 8 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2180-0 | 70518218000 | 90 in 1 BOTTLE, PLASTIC | | | | | | Historical |
| 70518-2180-1 | 70518218001 | 30 TABLET in 1 BLISTER PACK (70518-2180-1) | 30 tablet | 2022-02-01 | 0000-00-00 | No | No | Current |
| 70518-2180-2 | 70518218002 | 30 TABLET in 1 BOTTLE, PLASTIC (70518-2180-2) | 30 tablet | 2025-10-17 | | No | No | Historical |