Venlafaxine Hydrochloride
- Product NDC
- 50090-1216
- 11-digit product format
- 500901216
- Labeler code
- 50090
- Product ID
- 50090-1216_e63d5134-b14c-4634-8a49-1537dfc2c2e5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076565
- Marketing category
- ANDA
- Marketing start
- 2010-07-01
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 150 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
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 50090-1216-0 | 2021-06-10 | C162847 | 48780-1 | 9d75b9d1-13b9-f424-e053-dadaa90a57ce | 50767b91-b9a0-497f-b863-c55e2d41d8d8 |
| 50090-1216-1 | 2021-06-10 | C162847 | 48780-1 | 9d75b9d1-13b9-f424-e053-dadaa90a57ce | 50767b91-b9a0-497f-b863-c55e2d41d8d8 |
| 50090-1216-0 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d1-13b9-f424-e053-dadaa90a57ce | 50767b91-b9a0-497f-b863-c55e2d41d8d8 |
| 50090-1216-1 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d1-13b9-f424-e053-dadaa90a57ce | 50767b91-b9a0-497f-b863-c55e2d41d8d8 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 50090-1216-0 | EA - Each | 50090-1216 | df2507f4-7e23-422e-8113-a5311eab8e7b | 1 | 2018-11-06 |
| 50090-1216-1 | EA - Each | 50090-1216 | 5f85fe64-5d7c-4153-a750-e3612e2fa9fa | 1 | 2018-11-06 |