Desvenlafaxine
- Product NDC
- 71335-1700
- 11-digit product format
- 713351700
- Labeler code
- 71335
- Product ID
- 71335-1700_4a9487ae-3632-40da-b2a7-238060205a74
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Desvenlafaxine
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA204082
- Marketing category
- ANDA
- Marketing start
- 2017-03-01
- Substance
- DESVENLAFAXINE SUCCINATE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Cytochrome P450 2D6 Inhibitors [MoA], Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
openFDA Listing Details
- Product ID
- 71335-1700_4a9487ae-3632-40da-b2a7-238060205a74
- SPL ID
- 4a9487ae-3632-40da-b2a7-238060205a74
- Product type
- HUMAN PRESCRIPTION DRUG
- Finished product
- Yes
- Brand name base
- Desvenlafaxine
- Generic name
- Desvenlafaxine
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Marketing start
- 2017-03-01
- Marketing category
- ANDA
- Application number
- ANDA204082
- Pharmacologic classes
- Cytochrome P450 2D6 Inhibitors [MoA]; Norepinephrine Uptake Inhibitors [MoA]; Serotonin Uptake Inhibitors [MoA]; Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
- Listing expiration
- 2027-12-31
openFDA Active Ingredients
| Ingredient | Strength |
|---|
| DESVENLAFAXINE SUCCINATE | 50 mg/1 |
openFDA Harmonized Identifiers
| Field | Values |
|---|
| Unii | ZB22ENF0XR |
| Rxcui | 1874559 |
| Spl Set Id | aca478a7-eff6-4cd5-93a8-2dca69883a4b |
| Manufacturer Name | Bryant Ranch Prepack |
openFDA Package Details
| Package NDC | Description | Marketing start | Sample |
|---|
| 71335-1700-1 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1700-1) | 2020-09-03 | No |
| 71335-1700-2 | 28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1700-2) | 2025-01-30 | No |
| 71335-1700-3 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1700-3) | 2025-01-30 | No |
| 71335-1700-4 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1700-4) | 2023-09-25 | No |
| 71335-1700-5 | 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1700-5) | 2025-01-30 | No |
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| ZB22ENF0XR | DESVENLAFAXINE SUCCINATE | 386750-22-7 | DESVENLAFAXINE SUCCINATE |
| NG99554ANW | DESVENLAFAXINE | 93413-62-8 | Desvenlafaxine |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-1700-1 | 71335170001 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1700-1) | 2020-09-03 | No | No | Historical |
| 71335-1700-2 | 71335170002 | 28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1700-2) | 2025-01-30 | No | No | Historical |
| 71335-1700-3 | 71335170003 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1700-3) | 2025-01-30 | No | No | Historical |
| 71335-1700-4 | 71335170004 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1700-4) | 2023-09-25 | No | No | Historical |
| 71335-1700-5 | 71335170005 | 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1700-5) | 2025-01-30 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Desvenlafaxine | Bryant Ranch Prepack | 2026-05-14 | HUMAN PRESCRIPTION DRUG LABEL | 5 |