Venlafaxine
- Product NDC
- 70710-1352
- 11-digit product format
- 707101352
- Labeler code
- 70710
- Product ID
- 70710-1352_479c565e-3c2f-42a1-8a19-b7a210e5f28d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Application
- ANDA215622
- Marketing category
- ANDA
- Marketing start
- 2022-09-01
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 225 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 | 225 mg/1 |
Harmonized Identifiers#
| Field | Values |
|---|---|
| Unii | 7D7RX5A8MO |
| Rxcui | 808744, 808748, 808751, 808753 |
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 |
|---|---|---|---|---|---|---|
| 70710-1352-1 | Venlafaxine | 100 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 100 | 2 | |
| 70710-1352-3 | Venlafaxine | 30 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 30 | 2 | |
| 70710-1352-9 | Venlafaxine | 90 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 90 | 2 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70710-1352-3 | EA - Each | 70710-1352 | e57d73bb-8827-4756-ab72-dab74166b2be | 1 | 2022-12-07 |
| 70710-1352-9 | EA - Each | 70710-1352 | 791d5e64-fb66-4e45-8a5c-ac6771e512b0 | 1 | 2022-12-07 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70710-1352 | VENLAFAXINE TABLET, EXTENDED RELEASE [ZYDUS PHARMACEUTICALS USA INC.] | 2 | Current NDC, Legacy NDC, 3 package rows | 20230903_db1d16b3-d1a2-4f41-adff-a87c17689aa0.zip |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 808744 | venlafaxine HCl 150 MG 24HR Extended Release Oral Tablet | PSN | db1d16b3-d1a2-4f41-adff-a87c17689aa0 | 2 |
| 808748 | venlafaxine HCl 225 MG 24HR Extended Release Oral Tablet | PSN | db1d16b3-d1a2-4f41-adff-a87c17689aa0 | 2 |
| 808751 | venlafaxine HCl 37.5 MG 24HR Extended Release Oral Tablet | PSN | db1d16b3-d1a2-4f41-adff-a87c17689aa0 | 2 |
| 808753 | venlafaxine HCl 75 MG 24HR Extended Release Oral Tablet | PSN | db1d16b3-d1a2-4f41-adff-a87c17689aa0 | 2 |
| 808744 | 24 HR venlafaxine 150 MG Extended Release Oral Tablet | SCD | db1d16b3-d1a2-4f41-adff-a87c17689aa0 | 2 |
| 808748 | 24 HR venlafaxine 225 MG Extended Release Oral Tablet | SCD | db1d16b3-d1a2-4f41-adff-a87c17689aa0 | 2 |
| 808751 | 24 HR venlafaxine 37.5 MG Extended Release Oral Tablet | SCD | db1d16b3-d1a2-4f41-adff-a87c17689aa0 | 2 |
| 808753 | 24 HR venlafaxine 75 MG Extended Release Oral Tablet | SCD | db1d16b3-d1a2-4f41-adff-a87c17689aa0 | 2 |
| 808744 | venlafaxine 150 MG (as venlafaxine hydrochloride) 24 HR Extended Release Oral Tablet | SY | db1d16b3-d1a2-4f41-adff-a87c17689aa0 | 2 |
| 808744 | venlafaxine 150 MG 24 HR Extended Release Oral Tablet | SY | db1d16b3-d1a2-4f41-adff-a87c17689aa0 | 2 |
| 808748 | venlafaxine 225 MG (as venlafaxine hydrochloride) 24 HR Extended Release Oral Tablet | SY | db1d16b3-d1a2-4f41-adff-a87c17689aa0 | 2 |
| 808748 | venlafaxine 225 MG 24 HR Extended Release Oral Tablet | SY | db1d16b3-d1a2-4f41-adff-a87c17689aa0 | 2 |
| 808751 | venlafaxine 37.5 MG (as venlafaxine hydrochloride) 24 HR Extended Release Oral Tablet | SY | db1d16b3-d1a2-4f41-adff-a87c17689aa0 | 2 |
| 808751 | venlafaxine 37.5 MG 24 HR Extended Release Oral Tablet | SY | db1d16b3-d1a2-4f41-adff-a87c17689aa0 | 2 |
| 808753 | venlafaxine 75 MG (as venlafaxine hydrochloride) 24 HR Extended Release Oral Tablet | SY | db1d16b3-d1a2-4f41-adff-a87c17689aa0 | 2 |
| 808753 | venlafaxine 75 MG 24 HR Extended Release Oral Tablet | SY | db1d16b3-d1a2-4f41-adff-a87c17689aa0 | 2 |
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 70710-1352-1 | 70710135201 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70710-1352-1) | 2022-09-01 | 0000-00-00 | No | No | Current |
| 70710-1352-3 | 70710135203 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70710-1352-3) | 2022-09-01 | 0000-00-00 | No | No | Current |
| 70710-1352-9 | 70710135209 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70710-1352-9) | 2022-09-01 | 0000-00-00 | No | No | Current |