Venlafaxine Hydrochloride
- Product NDC
- 0527-2604
- 11-digit product format
- 005272604
- Labeler code
- 0527
- Product ID
- 0527-2604_22da933d-33b2-43fa-b30f-bc0e599e99ac
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lannett Company, Inc.
- Application
- ANDA209193
- Marketing category
- ANDA
- Marketing start
- 2019-12-26
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 150 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0527-2604 | VENLAFAXINE HYDROCHLORIDE TABLET [LANNETT COMPANY, INC.] | 7 | Legacy NDC | 20220209_eda2cf78-3369-4463-b297-62c7edaa1314.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0527-2604-32 | 00527260432 | 30 TABLET in 1 BOTTLE (0527-2604-32) | 30 tablet | 2019-12-26 | 0000-00-00 | No | No | Current |
| 0527-2604-46 | 00527260446 | 90 TABLET in 1 BOTTLE (0527-2604-46) | 90 tablet | 2019-12-26 | 0000-00-00 | No | No | Current |