Venlafaxine Hydrochloride
- Product NDC
- 63629-2100
- 11-digit product format
- 636292100
- Labeler code
- 63629
- Product ID
- 63629-2100_c03a4815-4a12-4abb-aa11-0b1b078929da
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA209193
- Marketing category
- ANDA
- Marketing start
- 2019-10-31
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 150 mg/1
- Pharmacologic classes
- Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine 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
- Venlafaxine Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients
| Ingredient | Strength |
|---|
| VENLAFAXINE HYDROCHLORIDE | 150 mg/1 |
Harmonized Identifiers
| Field | Values |
|---|
| Unii | 7D7RX5A8MO |
| Rxcui | 808744 |
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 7D7RX5A8MO | VENLAFAXINE HYDROCHLORIDE | 99300-78-4 | VENLAFAXINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-2100-1 | 63629210001 | 30 TABLET in 1 BOTTLE (63629-2100-1) | 30 tablet | 2019-10-31 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Venlafaxine Hydrochloride | Bryant Ranch Prepack | 2023-02-27 | HUMAN PRESCRIPTION DRUG LABEL | 103 |