Prescription drug · ANDA
Venlafaxine NDC 71209-089
Venlafaxine hydrochloride 225 mg/1 · Tablet, Coated · Oral · Cadila Pharmaceuticals Limited
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71209-089-01 | 71209008901 | 30 TABLET, COATED in 1 BOTTLE (71209-089-01)Marketed from Aug 16, 2018 | |
| 71209-089-04 | 71209008904 | 90 TABLET, COATED in 1 BOTTLE (71209-089-04)Marketed from Aug 16, 2018 | |
| 71209-089-11 | 71209008911 | 1000 TABLET, COATED in 1 BOTTLE (71209-089-11)Marketed from Aug 16, 2018 |
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
- Active ingredients
- Venlafaxine hydrochloride — 225 mg/1
- Dosage form
- Tablet, Coated
- Route
- Oral
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 211323
- Marketing start
- Listing expires
- Other FDA classes
- Norepinephrine Uptake Inhibitors (Mechanism)Serotonin Uptake Inhibitors (Mechanism)
- Identifiers
- Product ID 71209-089_5e8d05f3-2a6f-4132-b7e3-9dc90804f2d3SPL ID 5e8d05f3-2a6f-4132-b7e3-9dc90804f2d3SPL set ID 516e7566-35c2-4a25-88d8-54d9dbc8f6beRxCUI 808744, 808748, 808753UNII 7D7RX5A8MOUPC 0371209087117, 0371209089111
- 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
N471209008901followed by a unit qualifier and the quantityPackage 71209-0089-01. 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 211323
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 | Venlafaxine hydrochloride 75 mg/1 | Tablet, CoatedOral | Modavar Pharmaceuticals LLC | 72241-075 |
| Venlafaxine | Venlafaxine hydrochloride 150 mg/1 | Tablet, CoatedOral | Modavar Pharmaceuticals LLC | 72241-076 |
| Venlafaxine | Venlafaxine hydrochloride 225 mg/1 | Tablet, CoatedOral | Modavar Pharmaceuticals LLC | 72241-077 |
| Venlafaxine Hydrochloride | Venlafaxine hydrochloride 75 mg/1 | Tablet, Extended releaseOral | Nivagen Pharmaceuticals, Inc. | 75834-217 |
| Venlafaxine Hydrochloride | Venlafaxine hydrochloride 150 mg/1 | Tablet, Extended releaseOral | Nivagen Pharmaceuticals, Inc. | 75834-218 |
| Venlafaxine Hydrochloride | Venlafaxine hydrochloride 225 mg/1 | Tablet, Extended releaseOral | Nivagen Pharmaceuticals, Inc. | 75834-219 |
| Venlafaxine | Venlafaxine hydrochloride 150 mg/1 | Tablet, CoatedOral | Cadila Pharmaceuticals Limited | 71209-088 |
| Venlafaxine | Venlafaxine hydrochloride 75 mg/1 | Tablet, CoatedOral | Cadila Pharmaceuticals Limited | 71209-087 |