What is NDC 0121-1076?

0121-1076 is the product NDC for Mupirocin, Mupirocin 20 mg/g ointment, listed with the FDA by PAI Holdings, LLC dba PAI Pharma. It has 1 package NDC, shown above in 10- and 11-digit form.

PAI Holdings, LLC dba PAI Pharma, NDC labeler code 0121. 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 0121-1076 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)0121-1076Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00121-1076Add 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
0121-1076-50	0012110765000121107650	50 TUBE in 1 CARTON (0121-1076-50) / 1 g in 1 TUBE (0121-1076-01)Marketed from Mar 13, 2026

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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): Mupirocin
Generic name (nonproprietary): mupirocin
Active ingredients: Mupirocin — 20 mg/g
Dosage form: Ointment
Route: Topical
Labeler: PAI Holdings, LLC dba PAI PharmaNDC labeler code 0121
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 065170
Marketing start: Mar 13, 2026
Listing expires: Dec 31, 2027
Other FDA classes: RNA Synthetase Inhibitors (Mechanism)
Identifiers: Product ID 0121-1076_8427d472-619e-41ef-ae3c-a534b8a9255bSPL ID 8427d472-619e-41ef-ae3c-a534b8a9255bSPL set ID a822d44d-c651-406c-a2b9-aa8fbe8f89ceRxCUI 106346UNII D0GX863OA5
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

N400121107650 followed by a unit qualifier and the quantity

Package 00121-1076-50. 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 Mar 17, 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 0121-1076

What is NDC 0121-1076?: 0121-1076 is the product NDC for Mupirocin, Mupirocin 20 mg/g ointment, listed with the FDA by PAI Holdings, LLC dba PAI Pharma. 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?: PAI Holdings, LLC dba PAI Pharma, NDC labeler code 0121. 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
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 20 mg/g	OintmentTopical	Redpharm Drug	67296-2211	67296-2211-01
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 065170

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

FDA NDC Directory listings under ANDA 065170
Product	Strength	Form · route	Labeler	Product NDC
Mupirocin	Mupirocin 20 mg/g	OintmentTopical	AvPAK	50268-568
Mupirocin	Mupirocin 20 mg/g	OintmentTopical	Sun Pharmaceutical Industries, Inc.	51672-1312
Mupirocin	Mupirocin 20 mg/g	OintmentTopical	Proficient Rx LP	63187-151
Mupirocin	Mupirocin 20 mg/g	OintmentTopical	NuCare Pharmaceuticals,Inc.	68071-4321
Mupirocin	Mupirocin 20 mg/g	OintmentTopical	Lohxa	70166-355
Mupirocin	Mupirocin 20 mg/g	OintmentTopical	Advanced Rx Pharmacy of Tennessee, LLC	80425-0254
Mupirocin	Mupirocin 20 mg/g	OintmentTopical	Sportpharm LLC	85766-207