Venlafaxine Hydrochloride
- Product NDC
- 55700-914
- 11-digit product format
- 557000914
- Labeler code
- 55700
- Product ID
- 55700-914_b55f3cc1-72a4-45c4-94bf-7b2166e04fcc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA212277
- Marketing category
- ANDA
- Marketing start
- 2021-06-11
- 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 |
|---|
| 55700-914 | VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE [QUALITY CARE PRODUCTS, LLC] | 6 | Legacy NDC | 20241220_c5ed435f-e57b-4262-ad56-b2c6b226ba95.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-914-30 | 55700091430 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55700-914-30) | 2021-06-11 | 0000-00-00 | No | No | Current |
| 55700-914-90 | 55700091490 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55700-914-90) | 2022-02-17 | 0000-00-00 | No | No | Current |