Venlafaxine Hydrochloride
- Product NDC
- 60760-121
- 11-digit product format
- 607600121
- Labeler code
- 60760
- Product ID
- 60760-121_ef538879-d19d-4f2b-e053-2995a90a4588
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Marys Medical Park Pharmacy
- Application
- ANDA077653
- Marketing category
- ANDA
- Marketing start
- 2011-01-30
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 75 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 Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60760-121 | VENLAFAXINE HYDROCHLORIDE TABLET [ST. MARYS MEDICAL PARK PHARMACY] | 5 | Legacy NDC | 20221209_341720f7-f76f-498b-856f-3d207ad63feb.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-121-30 | 60760012130 | 30 TABLET in 1 BOTTLE, PLASTIC (60760-121-30) | 30 tablet | 2011-01-30 | 0000-00-00 | No | No | Current |