Venlafaxine Hydrochloride
- Product NDC
- 21695-720
- 11-digit product format
- 216950720
- Labeler code
- 21695
- Product ID
- 21695-720_2016f03e-e7ac-43b6-8244-0389ce057b2b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rebel Distributors Corp.
- Application
- ANDA076690
- Marketing category
- ANDA
- Marketing start
- 2009-09-03
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
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 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 21695-720-60 | 2019-09-24 | C162847 | 48780-1 | 934fe258-49aa-48b1-e053-8cdaa90a720a | VENLAFAXINE HYDROCHLORIDE TABLETS 0199 7380 7381 7382 7383 Rx only |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 21695-720-60 | Venlafaxine Hydrochloride | 60 in 1 BOTTLE | TABLET | 60 | 2 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 21695-720-60 | EA - Each | 21695-720 | c7d2c1a6-b866-4aa0-ba33-afd4b79ae28c | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| VENLAFAXINE HYDROCHLORIDE | ACTIVE INGREDIENT | 7D7RX5A8MO | VENLAFAXINE HYDROCHLORIDE TABLET [REBEL DISTRIBUTORS CORP.] | 2 | |
| VENLAFAXINE | ACTIVE MOIETY | GRZ5RCB1QG | VENLAFAXINE HYDROCHLORIDE TABLET [REBEL DISTRIBUTORS CORP.] | 2 |
DailyMed Dashboard NDC Coverage#
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 313580 | venlafaxine HCl 100 MG Oral Tablet | PSN | 49bef388-71ff-43b1-87a8-9fd506a0e63e | 2 |
| 313582 | venlafaxine HCl 25 MG Oral Tablet | PSN | 49bef388-71ff-43b1-87a8-9fd506a0e63e | 2 |
| 313584 | venlafaxine HCl 37.5 MG Oral Tablet | PSN | 49bef388-71ff-43b1-87a8-9fd506a0e63e | 2 |
| 313586 | venlafaxine HCl 75 MG Oral Tablet | PSN | 49bef388-71ff-43b1-87a8-9fd506a0e63e | 2 |
| 313580 | venlafaxine 100 MG Oral Tablet | SCD | 49bef388-71ff-43b1-87a8-9fd506a0e63e | 2 |
| 313582 | venlafaxine 25 MG Oral Tablet | SCD | 49bef388-71ff-43b1-87a8-9fd506a0e63e | 2 |
| 313584 | venlafaxine 37.5 MG Oral Tablet | SCD | 49bef388-71ff-43b1-87a8-9fd506a0e63e | 2 |
| 313586 | venlafaxine 75 MG Oral Tablet | SCD | 49bef388-71ff-43b1-87a8-9fd506a0e63e | 2 |
| 313580 | venlafaxine 100 MG (as venlafaxine hydrochloride 113 MG) Oral Tablet | SY | 49bef388-71ff-43b1-87a8-9fd506a0e63e | 2 |
| 313582 | venlafaxine 25 MG (as venlafaxine hydrochloride 28.3 MG) Oral Tablet | SY | 49bef388-71ff-43b1-87a8-9fd506a0e63e | 2 |
| 313584 | venlafaxine 37.5 MG (as venlafaxine hydrochloride 42.5 MG) Oral Tablet | SY | 49bef388-71ff-43b1-87a8-9fd506a0e63e | 2 |
| 313586 | venlafaxine 75 MG (as venlafaxine hydrochloride 84.9 MG) Oral Tablet | SY | 49bef388-71ff-43b1-87a8-9fd506a0e63e | 2 |
Packages#
| Package NDC | 11-digit format | Description | Status |
|---|---|---|---|
| 21695-720-60 | 21695072060 | 60 in 1 BOTTLE | Historical |