What is NDC 51672-4118?

51672-4118 is the product NDC for Fluorouracil, Fluorouracil 50 mg/g cream, listed with the FDA by Sun Pharmaceutical Industries, Inc.. It has 3 package NDCs, 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 Fluorouracil?

40 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Fluorouracil NDC 51672-4118 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)51672-4118Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51672-4118Add 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
51672-4118-2	5167241180251672411802	1 TUBE in 1 CARTON (51672-4118-2) / 25 g in 1 TUBEMarketed from Mar 17, 2017
51672-4118-5	5167241180551672411805	5 g in 1 TUBE (51672-4118-5)Marketed from Mar 17, 2017
51672-4118-6	5167241180651672411806	1 TUBE in 1 CARTON (51672-4118-6) / 40 g in 1 TUBEMarketed from Mar 17, 2017

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): Fluorouracil
Generic name (nonproprietary): fluorouracil
Active ingredients: Fluorouracil — 50 mg/g
Dosage form: Cream
Route: Topical
Labeler: Sun Pharmaceutical Industries, Inc.NDC labeler code 51672
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 090368
Marketing start: Mar 5, 2010
Listing expires: Dec 31, 2027
Other FDA classes: Nucleic Acid Synthesis Inhibitors (Mechanism)
Identifiers: Product ID 51672-4118_569a2172-d3a9-45c5-e063-6394a90a3955SPL ID 569a2172-d3a9-45c5-e063-6394a90a3955SPL set ID acca0036-f19c-459b-9dfc-9592f1cd588dRxCUI 105583UNII U3P01618RT
Pharmacologic class: Nucleoside Metabolic 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. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N451672411802 followed by a unit qualifier and the quantity

Package 51672-4118-02. 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 Jul 14, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE Fluorouracil is recommended for the topical treatment of multiple actinic or solar keratoses. In the 5% strength, it is also useful in the treatment of superficial basal cell carcinomas when conventional methods are impractical, such as with multiple lesions or difficult treatment sites. Safety and efficacy in other indications have not been established. The diagnosis should be established prior to treatment, since this method has not been proven effective in other types of basal cell carcinomas. With isolated, easily accessible basal cell carcinomas, surgery is preferred since success with such lesions is almost 100%. The success rate with fluorouracil cream and soluti…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 51672-4118

What is NDC 51672-4118?: 51672-4118 is the product NDC for Fluorouracil, Fluorouracil 50 mg/g cream, listed with the FDA by Sun Pharmaceutical Industries, Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Fluorouracil.
What is the active ingredient?: Fluorouracil.
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 Fluorouracil?: 40 other product NDCs are listed under this name. See all Fluorouracil 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 Fluorouracil NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Fluorouracil	Fluorouracil 50 mg/mL	Injection, SolutionIntravenous	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-972	23155-0972-41
Fluorouracil	Fluorouracil 50 mg/mL	Injection, SolutionIntravenous	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-973	23155-0973-41
Fluorouracil	Fluorouracil 50 mg/mL	Injection, SolutionIntravenous	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-974	23155-0974-31
Fluorouracil	Fluorouracil 50 mg/mL	Injection, SolutionIntravenous	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-975	23155-0975-31
Fluorouracilfluorouracil cream, 0.5%	Fluorouracil 5 mg/g	CreamTopical	Dr. Reddy's Laboratories Inc.	75907-169	75907-0169-11
Fluorouracil	Fluorouracil 2 g/40g	CreamTopical	Encube Ethicals, Inc.	21922-049	21922-0049-17
Fluorouracil	Fluorouracil 50 mg/mL	Injection, SolutionIntravenous	Meitheal Pharmaceuticals Inc.	71288-154	71288-0154-76
Fluorouracil	Fluorouracil 50 mg/mL	Injection, SolutionIntravenous	BluePoint Laboratories	68001-628	68001-0628-32
Fluorouracil	Fluorouracil 50 mg/mL	Injection, SolutionIntravenous	BluePoint Laboratories	68001-627	68001-0627-27
Fluorouracil	Fluorouracil 50 mg/mL	Injection, SolutionIntravenous	Meitheal Pharmaceuticals Inc.	71288-170	71288-0170-75

All 41 Fluorouracil NDCs

Other NDCs under ANDA 090368

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

FDA NDC Directory listings under ANDA 090368
Product	Strength	Form · route	Labeler	Product NDC
Fluorouracil	Fluorouracil 50 mg/g	CreamTopical	NORTHSTAR RX LLC	16714-178