Venlafaxine Hydrochloride
- Product NDC
- 63629-2100
- 11-digit product format
- 636292100
- Labeler code
- 63629
- Product ID
- 63629-2100_c03a4815-4a12-4abb-aa11-0b1b078929da
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA209193
- Marketing category
- ANDA
- Marketing start
- 2019-10-31
- 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
- 2026-12-31
- Current FDA listing
- Yes
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63629-2100-1 | Venlafaxine Hydrochloride | 30 in 1 BOTTLE | TABLET | 30 | | 103 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-2100 | VENLAFAXINE HYDROCHLORIDE TABLET [BRYANT RANCH PREPACK] | 103 | Current NDC, Legacy NDC, 1 package rows | 20230228_5d184d1b-67fe-4965-bf3d-b49646df4f92.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 |
|---|
| 63629-2100-1 | 63629210001 | 30 TABLET in 1 BOTTLE (63629-2100-1) | 30 tablet | 2019-10-31 | 0000-00-00 | No | No | Current |