What is NDC 51672-4196?

51672-4196 is the product NDC for Deferiprone, Deferiprone 500 mg/1 tablet, listed with the FDA by Sun Pharmaceutical Industries, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

Sun Pharmaceutical Industries, Inc., NDC labeler code 51672. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Deferiprone?

6 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Deferiprone NDC 51672-4196 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)51672-4196Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51672-4196Add 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
51672-4196-1	5167241960151672419601	100 TABLET in 1 BOTTLE (51672-4196-1)Marketed from Feb 5, 2024

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): Deferiprone
Generic name (nonproprietary): deferiprone
Active ingredients: Deferiprone — 500 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Sun Pharmaceutical Industries, Inc.NDC labeler code 51672
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 208800
Marketing start: Feb 5, 2024
Listing expires: Dec 31, 2027
Other FDA classes: Iron Chelating Activity (Mechanism)
Identifiers: Product ID 51672-4196_3631d351-4653-3512-e063-6394a90a81c0SPL ID 3631d351-4653-3512-e063-6394a90a81c0SPL set ID 5af1643d-4c6e-4668-ae9b-1046f0ad6d8aRxCUI 389242, 2180997UNII 2BTY8KH53L
Pharmacologic class: Iron Chelator

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

N451672419601 followed by a unit qualifier and the quantity

Package 51672-4196-01. 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

Current FDA label (SPL), effective May 28, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

Deferiprone tablets are indicated for the treatment of transfusional iron overload in adult patients with thalassemia syndromes when current chelation therapy is inadequate. Deferiprone tablets are an iron chelator indicated for the treatment of transfusional iron overload in adult patients with thalassemia syndromes when current chelation therapy is inadequate. ( 1 ) Limitations of Use Safety and effectiveness have not been established for the treatment of transfusional iron overload in patients with myelodysplastic syndrome or in patients with Diamond Blackfan anemia. Limitations of Use Safety and effectiveness have not been established for the treatment of transfusional iron overload in p…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 51672-4196

What is NDC 51672-4196?: 51672-4196 is the product NDC for Deferiprone, Deferiprone 500 mg/1 tablet, listed with the FDA by Sun Pharmaceutical Industries, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Deferiprone.
What is the active ingredient?: Deferiprone.
Who is the labeler?: Sun Pharmaceutical Industries, Inc., NDC labeler code 51672. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Deferiprone?: 6 other product NDCs are listed under this name. See all Deferiprone NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Deferiprone NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Deferiprone	Deferiprone 500 mg/1	TabletOral	AvKARE	73190-095	73190-0095-01
Deferiprone	Deferiprone 1000 mg/1	Tablet, CoatedOral	DR. REDDY'S LABORATORIES, INC.	75907-348	75907-0348-50
Deferiprone	Deferiprone 500 mg/1	Tablet, CoatedOral	DR. REDDY'S LABORATORIES, INC.	75907-349	75907-0349-01
Deferiprone	Deferiprone 1000 mg/1	TabletOral	Sun Pharmaceutical Industries, Inc.	51672-4237	51672-4237-04
Deferiprone	Deferiprone 1000 mg/1	Tablet, CoatedOral	Hikma Pharmaceuticals USA Inc.	0054-0711	00054-0711-1900054-0711-2300054-0711-28
Deferiprone	Deferiprone 500 mg/1	Tablet, CoatedOral	Hikma Pharmaceuticals USA Inc.	0054-0576	00054-0576-25

Other NDCs under ANDA 208800

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

FDA NDC Directory listings under ANDA 208800
Product	Strength	Form · route	Labeler	Product NDC
Deferiprone	Deferiprone 1000 mg/1	TabletOral	Sun Pharmaceutical Industries, Inc.	51672-4237
Deferiprone	Deferiprone 500 mg/1	TabletOral	AvKARE	73190-095