VENLAFAXINE
- Product NDC
- 61919-804
- 11-digit product format
- 619190804
- Labeler code
- 61919
- Product ID
- 61919-804_87e71680-68de-7a37-e053-2a95a90af7f0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- VENLAFAXINE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA090555
- Marketing category
- ANDA
- Marketing start
- 2019-05-02
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 75 mg/1
- Pharmacologic classes
- Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 61919-804-30 | VENLAFAXINE | 30 in 1 BOTTLE | TABLET | 30 | | 9 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-804 | VENLAFAXINE TABLET VENLAFAXINE TABLET [DIRECT RX] | 9 | Legacy NDC, 1 package rows | 20230411_5cdfdcb3-eaa5-63b9-e053-2a91aa0ae17f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 61919-804-30 | 61919080430 | 30 in 1 BOTTLE | Historical |