What is NDC 67296-2211?

67296-2211 is the product NDC for Mupirocin, Mupirocin 20 mg/g ointment, listed with the FDA by Redpharm Drug. It has 1 package NDC, shown above in 10- and 11-digit form.

Redpharm Drug, NDC labeler code 67296. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Mupirocin?

42 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Mupirocin NDC 67296-2211 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)67296-2211Labeler and product segments. Claims need a package NDC.

Product NDC at billing width67296-2211Add 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
67296-2211-1	6729622110167296221101	1 TUBE in 1 CARTON (67296-2211-1) / 22 g in 1 TUBEMarketed from May 16, 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): Mupirocin
Generic name (nonproprietary): mupirocin
Active ingredients: Mupirocin — 20 mg/g
Dosage form: Ointment
Route: Topical
Labeler: Redpharm DrugNDC labeler code 67296
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 217943
Marketing start: May 16, 2025
Listing expires: Dec 31, 2027
Other FDA classes: RNA Synthetase Inhibitors (Mechanism)
Identifiers: Product ID 67296-2211_49eb7298-0834-2baa-e063-6394a90a7b4aSPL ID 49eb7298-0834-2baa-e063-6394a90a7b4aSPL set ID 49eb7289-c44d-75e1-e063-6294a90a2283RxCUI 106346UNII D0GX863OA5UPC 0321922073041, 0321922073058, 0321922073256
Pharmacologic class: RNA Synthetase Inhibitor Antibacterial

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

N467296221101 followed by a unit qualifier and the quantity

Package 67296-2211-01. 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 Feb 3, 2026.

Indications (excerpt from the label)

Mupirocin Ointment USP, 2% is indicated for the topical treatment of impetigo due to susceptible isolates of Staphylococcus aureus (S. aureus) and Streptococcus pyogenes (S. pyogenes) . Mupirocin ointment is an RNA synthetase inhibitor antibacterial indicated for the topical treatment of impetigo due to susceptible isolates of Staphylococcus aureus and Streptococcus pyogenes. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 67296-2211

What is NDC 67296-2211?: 67296-2211 is the product NDC for Mupirocin, Mupirocin 20 mg/g ointment, listed with the FDA by Redpharm Drug. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Mupirocin.
What is the active ingredient?: Mupirocin.
Who is the labeler?: Redpharm Drug, NDC labeler code 67296. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Mupirocin?: 42 other product NDCs are listed under this name. See all Mupirocin 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 Mupirocin NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Mupirocin	Mupirocin calcium 20 mg/g	CreamTopical	Zydus Lifesciences Limited	70771-1981	70771-1981-0170771-1981-02
Mupirocin	Mupirocin calcium 20 mg/g	CreamTopical	Viona Pharmaceuticals Inc	72578-130	72578-0130-0172578-0130-06
Mupirocin	Mupirocin 20 mg/g	OintmentTopical	PAI Holdings, LLC dba PAI Pharma	0121-1076	00121-1076-50
Mupirocinmupirocin ointment	Mupirocin 20 mg/g	OintmentTopical	Kesin Pharma Corporation	81033-032	81033-0032-5081033-0032-99
Mupirocin	Mupirocin 20 mg/g	OintmentTopical	Encube Ethicals, Inc.	21922-073	21922-0073-0421922-0073-0521922-0073-25
Mupirocin	Mupirocin calcium 20 mg/g	CreamTopical	Alembic Pharmaceuticals Limited	46708-624	46708-0624-1546708-0624-30
mupirocin	Mupirocin 20 mg/g	OintmentTopical	St. Mary's Medical Park Pharmacy	60760-960	60760-0960-22
mupirocin	Mupirocin 20 mg/g	OintmentTopical	Preferred Pharmaceuticals Inc.	68788-8642	68788-8642-02
Mupirocin	Mupirocin 20 mg/g	OintmentTopical	Preferred Pharmaceuticals Inc.	68788-8534	68788-8534-02
Mupirocinmupirocin calcium	Mupirocin calcium 20 mg/g	CreamTopical	REMEDYREPACK INC.	70518-3774	70518-3774-00

All 43 Mupirocin NDCs

Other NDCs under ANDA 217943

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

FDA NDC Directory listings under ANDA 217943
Product	Strength	Form · route	Labeler	Product NDC
Mupirocin	Mupirocin 20 mg/g	OintmentTopical	Encube Ethicals, Inc.	21922-073