Anagrelide NDC 62135-312

NDC codes

FDA NDC Directory

Product NDC (as listed)62135-312Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62135-0312Add 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 NDC	11-digit (billing)	Package	Copy
62135-312-12	62135031212	120 CAPSULE in 1 BOTTLE (62135-312-12)Marketed from Feb 5, 2024

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): Anagrelide
Generic name (nonproprietary): anagrelide
Active ingredients: Anagrelide hydrochloride anhydrous — .5 mg/1
Dosage form: Capsule
Route: Oral
Labeler: Chartwell RX, LLC
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 076683
Marketing start: Apr 18, 2005
Listing expires: Dec 31, 2026
Other FDA classes: Decreased Platelet Production (Physiologic effect)Phosphodiesterase 3 Inhibitors (Mechanism)
Identifiers: Product ID 62135-312_13156e50-28d1-0994-e063-6394a90a16ecSPL ID 13156e50-28d1-0994-e063-6394a90a16ecSPL set ID e031dfb3-56e1-4fea-95f2-c2936e2057a0RxCUI 597850, 597852UNII VNS4435G39UPC 0362135312121, 0362135313609
Pharmacologic class: Platelet-reducing Agent

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

N462135031212 followed by a unit qualifier and the quantity

Package 62135-0312-12. 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 076683

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

FDA NDC Directory listings under ANDA 076683
Product	Strength	Form · route	Labeler	Product NDC
Anagrelide	Anagrelide hydrochloride anhydrous 1 mg/1	CapsuleOral	Chartwell RX, LLC	62135-313