venlafaxine
- Product NDC
- 53217-081
- 11-digit product format
- 532170081
- Labeler code
- 53217
- Product ID
- 53217-081_8a6f6dc6-2dc8-454b-bf65-02888cddb0e4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- venlafaxine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aidarex Pharmaceuticals LLC
- Application
- ANDA078932
- Marketing category
- ANDA
- Marketing start
- 2015-10-01
- 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
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 53217-081-30 | venlafaxine | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
| 53217-081-60 | venlafaxine | 60 in 1 BOTTLE | TABLET | 60 | | 1 |
| 53217-081-90 | venlafaxine | 90 in 1 BOTTLE | TABLET | 90 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53217-081 | VENLAFAXINE TABLET [AIDAREX PHARMACEUTICALS LLC] | 1 | Legacy NDC, 3 package rows | 20170512_5c2e417d-8f09-4efc-86bf-d822c0471a90.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 53217-081-30 | 53217008130 | 30 in 1 BOTTLE | Historical |
| 53217-081-60 | 53217008160 | 60 in 1 BOTTLE | Historical |
| 53217-081-90 | 53217008190 | 90 in 1 BOTTLE | Historical |