Prescription drug · ANDA
venlafaxine (venlafaxine hydrochloride) NDC 51655-323
Venlafaxine hydrochloride 37.5 mg/1 · Tablet · Oral · Northwind Health Company, LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 51655-323-52 | 51655032352 | 30 TABLET in 1 BOTTLE, PLASTIC (51655-323-52)Marketed from May 2, 2023 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- venlafaxine
- Generic name (nonproprietary)
- venlafaxine hydrochloride
- Active ingredients
- Venlafaxine hydrochloride — 37.5 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 090555
- Marketing start
- Listing expires
- Other FDA classes
- Norepinephrine Uptake Inhibitors (Mechanism)Serotonin Uptake Inhibitors (Mechanism)
- Identifiers
- Product ID 51655-323_48eafbab-f3bb-58cd-e063-6394a90a1544SPL ID 48eafbab-f3bb-58cd-e063-6394a90a1544SPL set ID fb076577-b9da-c78b-e053-6394a90a107bRxCUI 313584UNII 7D7RX5A8MO
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N451655032352followed by a unit qualifier and the quantityPackage 51655-0323-52. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Label details couldn’t be retrieved right now. Open the label on DailyMed.
Other NDCs under ANDA 090555
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| venlafaxinevenlafaxine hydrochloride | Venlafaxine hydrochloride 100 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-1976 |
| venlafaxinevenlafaxine hydrochloride | Venlafaxine hydrochloride 37.5 mg/1 | TabletOral | Coupler LLC | 67046-0560 |
| Venlafaxinevenlafaxine hydrochloride | Venlafaxine hydrochloride 37.5 mg/1 | TabletOral | Aurobindo Pharma Limited | 65862-405 |
| Venlafaxinevenlafaxine hydrochloride | Venlafaxine hydrochloride 25 mg/1 | TabletOral | Aurobindo Pharma Limited | 65862-404 |
| Venlafaxinevenlafaxine hydrochloride | Venlafaxine hydrochloride 50 mg/1 | TabletOral | Aurobindo Pharma Limited | 65862-406 |
| Venlafaxinevenlafaxine hydrochloride | Venlafaxine hydrochloride 75 mg/1 | TabletOral | Aurobindo Pharma Limited | 65862-407 |
| Venlafaxinevenlafaxine hydrochloride | Venlafaxine hydrochloride 100 mg/1 | TabletOral | Aurobindo Pharma Limited | 65862-408 |
| venlafaxinevenlafaxine hydrochloride | Venlafaxine hydrochloride 75 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-1104 |
| venlafaxinevenlafaxine hydrochloride | Venlafaxine hydrochloride 75 mg/1 | TabletOral | Northwind Health Company, LLC | 51655-223 |
| venlafaxinevenlafaxine hydrochloride | Venlafaxine hydrochloride 37.5 mg/1 | TabletOral | A-S Medication Solutions | 50090-4853 |
| venlafaxinevenlafaxine hydrochloride | Venlafaxine hydrochloride 37.5 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-1385 |
| venlafaxinevenlafaxine hydrochloride | Venlafaxine hydrochloride 37.5 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-1213 |
| venlafaxinevenlafaxine hydrochloride | Venlafaxine hydrochloride 75 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-2652 |
| venlafaxinevenlafaxine hydrochloride | Venlafaxine hydrochloride 25 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-2659 |
| venlafaxinevenlafaxine hydrochloride | Venlafaxine hydrochloride 25 mg/1 | TabletOral | Rising Pharma Holdings, Inc. | 57237-172 |
| venlafaxinevenlafaxine hydrochloride | Venlafaxine hydrochloride 75 mg/1 | TabletOral | Rising Pharma Holdings, Inc. | 57237-175 |
| venlafaxinevenlafaxine hydrochloride | Venlafaxine hydrochloride 37.5 mg/1 | TabletOral | Rising Pharma Holdings, Inc. | 57237-173 |
| venlafaxinevenlafaxine hydrochloride | Venlafaxine hydrochloride 50 mg/1 | TabletOral | Rising Pharma Holdings, Inc. | 57237-174 |
| venlafaxinevenlafaxine hydrochloride | Venlafaxine hydrochloride 100 mg/1 | TabletOral | Rising Pharma Holdings, Inc. | 57237-176 |
| venlafaxinevenlafaxine hydrochloride | Venlafaxine hydrochloride 50 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-1907 |