VENLAFAXINE HYDROCHLORIDE
- Product NDC
- 46708-792
- 11-digit product format
- 467080792
- Labeler code
- 46708
- Product ID
- 46708-792_e3e238db-4388-49bb-aa67-6d73adbb2280
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- VENLAFAXINE HYDROCHLORIDE
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Alembic Pharmaceuticals Limited
- Application
- ANDA217767
- Marketing category
- ANDA
- Marketing start
- 2024-06-10
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 37.5 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
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 | Marketing start | Sample | Exclude flag | Status |
|---|
| 46708-792-30 | 46708079230 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (46708-792-30) | 2024-06-10 | No | No | Historical |
| 46708-792-31 | 46708079231 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (46708-792-31) | 2024-06-10 | No | No | Historical |
| 46708-792-71 | 46708079271 | 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (46708-792-71) | 2024-06-10 | No | No | Historical |
| 46708-792-90 | 46708079290 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (46708-792-90) | 2024-06-10 | No | No | Historical |
| 46708-792-91 | 46708079291 | 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (46708-792-91) | 2024-06-10 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| VENLAFAXINE HYDROCHLORIDE | Alembic Pharmaceuticals Limited | 2024-06-11 | Human Prescription Drug Label | 1 |