Prescription drug · ANDA
Venlafaxine Hydrochloride (venlafaxine) NDC 31722-124
Venlafaxine hydrochloride 75 mg/1 · Tablet, Extended release · Oral · Camber Pharmaceuticals, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 31722-124-30 | 31722012430 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-124-30)Marketed from Oct 23, 2020 | |
| 31722-124-90 | 31722012490 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-124-90)Marketed from Oct 23, 2020 |
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 Hydrochloride
- Generic name (nonproprietary)
- venlafaxine
- Active ingredients
- Venlafaxine hydrochloride — 75 mg/1
- Dosage form
- Tablet, Extended release
- Route
- Oral
- Labeler
- Camber Pharmaceuticals, Inc.
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 214419
- Marketing start
- Listing expires
- Other FDA classes
- Norepinephrine Uptake Inhibitors (Mechanism)Serotonin Uptake Inhibitors (Mechanism)
- Identifiers
- Product ID 31722-124_495259b8-9f81-4b6e-aa51-d199aa0edfb8SPL ID 495259b8-9f81-4b6e-aa51-d199aa0edfb8SPL set ID 8c4ccc5c-f6a2-4ce3-8866-9e6b32b08fd3RxCUI 808744, 808748, 808751, 808753UNII 7D7RX5A8MOUPC 0331722126908, 0331722125307, 0331722126304, 0331722123907, 0331722123303, 0331722124300, 0331722124904, 0331722125901
- 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
N431722012430followed by a unit qualifier and the quantityPackage 31722-0124-30. 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 214419
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 |
|---|---|---|---|---|
| Venlafaxine Hydrochloridevenlafaxine | Venlafaxine hydrochloride 37.5 mg/1 | Tablet, Extended releaseOral | Camber Pharmaceuticals, Inc. | 31722-123 |
| Venlafaxine Hydrochloridevenlafaxine | Venlafaxine hydrochloride 75 mg/1 | Tablet, Extended releaseOral | BluePoint Laboratories | 68001-497 |
| Venlafaxine Hydrochloridevenlafaxine | Venlafaxine hydrochloride 37.5 mg/1 | Tablet, Extended releaseOral | BluePoint Laboratories | 68001-496 |
| Venlafaxine Hydrochloridevenlafaxine | Venlafaxine hydrochloride 225 mg/1 | Tablet, Extended releaseOral | Camber Pharmaceuticals, Inc. | 31722-126 |
| Venlafaxine Hydrochloridevenlafaxine | Venlafaxine hydrochloride 150 mg/1 | Tablet, Extended releaseOral | BluePoint Laboratories | 68001-498 |
| Venlafaxine Hydrochloridevenlafaxine | Venlafaxine hydrochloride 150 mg/1 | Tablet, Extended releaseOral | Camber Pharmaceuticals, Inc. | 31722-125 |
| Venlafaxine Hydrochloridevenlafaxine | Venlafaxine hydrochloride 225 mg/1 | Tablet, Extended releaseOral | BluePoint Laboratories | 68001-499 |
| Venlafaxine Hydrochloridevenlafaxine | Venlafaxine hydrochloride 75 mg/1 | Tablet, Extended releaseOral | XLCare Pharmaceuticals, Inc. | 72865-198 |
| Venlafaxine Hydrochloridevenlafaxine | Venlafaxine hydrochloride 37.5 mg/1 | Tablet, Extended releaseOral | XLCare Pharmaceuticals, Inc. | 72865-197 |
| Venlafaxine Hydrochloridevenlafaxine | Venlafaxine hydrochloride 150 mg/1 | Tablet, Extended releaseOral | XLCare Pharmaceuticals, Inc. | 72865-199 |
| Venlafaxine Hydrochloridevenlafaxine | Venlafaxine hydrochloride 225 mg/1 | Tablet, Extended releaseOral | XLCare Pharmaceuticals, Inc. | 72865-200 |
- openFDA data updated
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Reference information only. Verify codes and billing rules against the applicable payer and official source before submitting a claim. How Med-Code handles data.