NDC codes

FDA NDC Directory
Product NDC (as listed)63629-7524Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63629-7524Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
63629-7524-16362975240130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-7524-1)Marketed from Jan 24, 2025
63629-7524-26362975240260 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-7524-2)Marketed from Jan 24, 2025
63629-7524-36362975240390 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-7524-3)Marketed from Jan 24, 2025
63629-7524-463629752404120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-7524-4)Marketed from Jan 24, 2025

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
Desvenlafaxine
Generic name (nonproprietary)
desvenlafaxine
Active ingredients
Desvenlafaxine succinate — 25 mg/1
Dosage form
Tablet, Film coated, Extended release
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 204082
Marketing start
Listing expires
Other FDA classes
Cytochrome P450 2D6 Inhibitors (Mechanism)Norepinephrine Uptake Inhibitors (Mechanism)Serotonin Uptake Inhibitors (Mechanism)
Identifiers
Product ID 63629-7524_9f976ef0-7c5a-4b5a-bca2-5fecdd4006ccSPL ID 9f976ef0-7c5a-4b5a-bca2-5fecdd4006ccSPL set ID d585d916-2a5d-4baa-9c64-52b12313aba3RxCUI 1607617UNII ZB22ENF0XR

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

N463629752401 followed by a unit qualifier and the quantity

Package 63629-7524-01. 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 204082

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 204082
ProductStrengthForm · routeLabelerProduct NDC
DesvenlafaxineDesvenlafaxine succinate 50 mg/1Tablet, Film coated, Extended releaseOralBryant Ranch Prepack71335-1700
DesvenlafaxineDesvenlafaxine succinate 50 mg/1Tablet, Film coated, Extended releaseOralAmerican Health Packaging60687-607
DesvenlafaxineDesvenlafaxine succinate 50 mg/1Tablet, Film coated, Extended releaseOralA-S Medication Solutions50090-4806

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