Venlafaxine Hydrochloride
- Product NDC
- 68151-0308
- 11-digit product format
- 681510308
- Labeler code
- 68151
- Product ID
- 68151-0308_9feeedf4-555b-4ace-9319-a1ec39aa2321
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA076690
- Marketing category
- ANDA
- Marketing start
- 2006-08-04
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 25 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
- 2018-12-31
- 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 |
|---|---|---|---|---|---|
| 68151-0308-0 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-8bb4-f424-e053-dadaa90a57ce | Venlafaxine Tablets USP Rx only |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68151-0308-0 | Venlafaxine Hydrochloride | 1 in 1 PACKAGE | TABLET | 1 | 4 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| VENLAFAXINE HYDROCHLORIDE | ACTIVE INGREDIENT | 7D7RX5A8MO | VENLAFAXINE HYDROCHLORIDE TABLET [CARILION MATERIALS MANAGEMENT] | 2 | |
| VENLAFAXINE | ACTIVE MOIETY | GRZ5RCB1QG | VENLAFAXINE HYDROCHLORIDE TABLET [CARILION MATERIALS MANAGEMENT] | 2 | |
| FERRIC OXIDE RED | INACTIVE INGREDIENT | 1K09F3G675 | VENLAFAXINE HYDROCHLORIDE TABLET [CARILION MATERIALS MANAGEMENT] | 2 | |
| FERRIC OXIDE YELLOW | INACTIVE INGREDIENT | EX438O2MRT | VENLAFAXINE HYDROCHLORIDE TABLET [CARILION MATERIALS MANAGEMENT] | 2 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | VENLAFAXINE HYDROCHLORIDE TABLET [CARILION MATERIALS MANAGEMENT] | 2 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | VENLAFAXINE HYDROCHLORIDE TABLET [CARILION MATERIALS MANAGEMENT] | 2 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | VENLAFAXINE HYDROCHLORIDE TABLET [CARILION MATERIALS MANAGEMENT] | 2 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | VENLAFAXINE HYDROCHLORIDE TABLET [CARILION MATERIALS MANAGEMENT] | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 68151-0308 | VENLAFAXINE HYDROCHLORIDE TABLET [CARILION MATERIALS MANAGEMENT] | 4 | Legacy NDC, 1 package rows | 20170706_cfa3ade0-6831-426d-a02f-0314006647d7.zip |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 313582 | venlafaxine HCl 25 MG Oral Tablet | PSN | cfa3ade0-6831-426d-a02f-0314006647d7 | 4 |
| 313582 | venlafaxine 25 MG Oral Tablet | SCD | cfa3ade0-6831-426d-a02f-0314006647d7 | 4 |
| 313582 | venlafaxine 25 MG (as venlafaxine hydrochloride 28.3 MG) Oral Tablet | SY | cfa3ade0-6831-426d-a02f-0314006647d7 | 4 |
Packages#
| Package NDC | 11-digit format | Description | Status |
|---|---|---|---|
| 68151-0308-0 | 68151030800 | 1 in 1 PACKAGE | Historical |