Venlafaxine
- Product NDC
- 68084-896
- 11-digit product format
- 680840896
- Labeler code
- 68084
- Product ID
- 68084-896_1f401c77-b3c1-291d-e063-6394a90aa890
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA077653
- Marketing category
- ANDA
- Marketing start
- 2015-09-29
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 25 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
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| VENLAFAXINE HYDROCHLORIDE | 25 mg/1 |
Harmonized Identifiers#
| Field | Values |
|---|---|
| Unii | 7D7RX5A8MO |
| Rxcui | 313582, 313584, 313586 |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 17db3736-056c-48b9-b0f4-00fccabb14e6 | Product name | 5 | 20251118 |
| 7be8b949-f2c0-bdd8-e89d-8af92c1b2ead | Product name | 9 | 20250224 |
| b1435b59-059c-404b-a587-53656bf80e17 | Product name | 1 | 20230314 |
| 6005cd75-f7b1-d6be-3cb5-4bd30d5c4617 | Product name | 3 | 20190314 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68084-896-25 | Venlafaxine | 30 in 1 BOX, UNIT-DOSE | TABLET | 30 | 9 | |
| 68084-896-95 | Venlafaxine | 1 in 1 BLISTER PACK | TABLET | 1 | 9 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 68084-896-25 | EA - Each | 68084-896 | 923f6673-0749-4e20-adc0-178dc6bb6288 | 1 | 2015-10-02 |
| 68084-896-95 | EA - Each | 68084-896 | e45e6054-cc83-433d-b596-ee3a44e9087a | 1 | 2015-10-02 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| VENLAFAXINE HYDROCHLORIDE | ACTIVE INGREDIENT | 7D7RX5A8MO | VENLAFAXINE TABLET [AMERICAN HEALTH PACKAGING] | 1 | |
| VENLAFAXINE | ACTIVE MOIETY | GRZ5RCB1QG | VENLAFAXINE TABLET [AMERICAN HEALTH PACKAGING] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | VENLAFAXINE TABLET [AMERICAN HEALTH PACKAGING] | 1 | |
| FERRIC OXIDE RED | INACTIVE INGREDIENT | 1K09F3G675 | VENLAFAXINE TABLET [AMERICAN HEALTH PACKAGING] | 1 | |
| FERRIC OXIDE YELLOW | INACTIVE INGREDIENT | EX438O2MRT | VENLAFAXINE TABLET [AMERICAN HEALTH PACKAGING] | 1 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | VENLAFAXINE TABLET [AMERICAN HEALTH PACKAGING] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | VENLAFAXINE TABLET [AMERICAN HEALTH PACKAGING] | 1 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | VENLAFAXINE TABLET [AMERICAN HEALTH PACKAGING] | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 313582 | venlafaxine HCl 25 MG Oral Tablet | PSN | d8899628-6e1b-40c6-9bc8-553d91ae2d0c | 9 |
| 313584 | venlafaxine HCl 37.5 MG Oral Tablet | PSN | d8899628-6e1b-40c6-9bc8-553d91ae2d0c | 9 |
| 313586 | venlafaxine HCl 75 MG Oral Tablet | PSN | d8899628-6e1b-40c6-9bc8-553d91ae2d0c | 9 |
| 313582 | venlafaxine 25 MG Oral Tablet | SCD | d8899628-6e1b-40c6-9bc8-553d91ae2d0c | 9 |
| 313584 | venlafaxine 37.5 MG Oral Tablet | SCD | d8899628-6e1b-40c6-9bc8-553d91ae2d0c | 9 |
| 313586 | venlafaxine 75 MG Oral Tablet | SCD | d8899628-6e1b-40c6-9bc8-553d91ae2d0c | 9 |
| 313582 | venlafaxine 25 MG (as venlafaxine hydrochloride 28.3 MG) Oral Tablet | SY | d8899628-6e1b-40c6-9bc8-553d91ae2d0c | 9 |
| 313584 | venlafaxine 37.5 MG (as venlafaxine hydrochloride 42.5 MG) Oral Tablet | SY | d8899628-6e1b-40c6-9bc8-553d91ae2d0c | 9 |
| 313586 | venlafaxine 75 MG (as venlafaxine hydrochloride 84.9 MG) Oral Tablet | SY | d8899628-6e1b-40c6-9bc8-553d91ae2d0c | 9 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 68084-896-25 | 68084089625 | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-896-25) / 1 TABLET in 1 BLISTER PACK (68084-896-95) | 30 blister pack | 2015-09-29 | 0000-00-00 | No | No | Current |
| 68084-896-95 | 68084089695 | 1 in 1 BLISTER PACK | Historical |