NDC codes

FDA NDC Directory
Product NDC (as listed)60760-960Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60760-0960Add 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 NDC11-digit (billing)PackageCopy
60760-960-2260760096022607600960221 TUBE in 1 CARTON (60760-960-22) / 22 g in 1 TUBEMarketed from Sep 6, 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)
mupirocin
Generic name (nonproprietary)
mupirocin
Active ingredients
Mupirocin — 20 mg/g
Dosage form
Ointment
Route
Topical
Labeler
St. Mary's Medical Park PharmacyNDC labeler code 60760
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 065123
Marketing start
Listing expires
Other FDA classes
RNA Synthetase Inhibitors (Mechanism)
Identifiers
Product ID 60760-960_5500bf2e-918e-5b20-e063-6294a90a4a39SPL ID 5500bf2e-918e-5b20-e063-6294a90a4a39SPL set ID 235c4f77-e751-a69f-e063-6394a90a1f96RxCUI 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

N460760096022 followed by a unit qualifier and the quantity

Package 60760-0960-22. 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 .

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 USP, 2% is an RNA synthetase inhibitor antibacterial indicated for the topical treatment of impetigo due to susceptible isolates of Staphylococcus aureus and Streptococcus pyogenes.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 60760-960

What is NDC 60760-960?
60760-960 is the product NDC for mupirocin, Mupirocin 20 mg/g ointment, listed with the FDA by St. Mary's Medical Park Pharmacy. 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?
St. Mary's Medical Park Pharmacy, NDC labeler code 60760. 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
MupirocinMupirocin calcium 20 mg/gCreamTopicalZydus Lifesciences Limited70771-198170771-1981-0170771-1981-02
MupirocinMupirocin calcium 20 mg/gCreamTopicalViona Pharmaceuticals Inc72578-13072578-0130-0172578-0130-06
MupirocinMupirocin 20 mg/gOintmentTopicalPAI Holdings, LLC dba PAI Pharma0121-107600121-1076-50
Mupirocinmupirocin ointmentMupirocin 20 mg/gOintmentTopicalKesin Pharma Corporation81033-03281033-0032-5081033-0032-99
MupirocinMupirocin 20 mg/gOintmentTopicalEncube Ethicals, Inc.21922-07321922-0073-0421922-0073-0521922-0073-25
MupirocinMupirocin 20 mg/gOintmentTopicalRedpharm Drug67296-221167296-2211-01
MupirocinMupirocin calcium 20 mg/gCreamTopicalAlembic Pharmaceuticals Limited46708-62446708-0624-1546708-0624-30
mupirocinMupirocin 20 mg/gOintmentTopicalPreferred Pharmaceuticals Inc.68788-864268788-8642-02
MupirocinMupirocin 20 mg/gOintmentTopicalPreferred Pharmaceuticals Inc.68788-853468788-8534-02
Mupirocinmupirocin calciumMupirocin calcium 20 mg/gCreamTopicalREMEDYREPACK INC.70518-377470518-3774-00

All 43 mupirocin NDCs

Other NDCs under ANDA 065123

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

FDA NDC Directory listings under ANDA 065123
ProductStrengthForm · routeLabelerProduct NDC
mupirocinMupirocin 20 mg/gOintmentTopicalATLANTIC BIOLOGICALS CORP.17856-0112
mupirocinMupirocin 20 mg/gOintmentTopicalPadagis Israel Pharmaceuticals Ltd45802-112
mupirocinMupirocin 20 mg/gOintmentTopicalA-S Medication Solutions50090-1587
mupirocinMupirocin 20 mg/gOintmentTopicalProficient Rx LP63187-261
mupirocinMupirocin 20 mg/gOintmentTopicalBryant Ranch Prepack63629-8687
mupirocinMupirocin 20 mg/gOintmentTopicalNuCare Pharmaceuticals,Inc.68071-4789
mupirocinMupirocin 20 mg/gOintmentTopicalPreferred Pharmaceuticals Inc.68788-8642
mupirocinMupirocin 20 mg/gOintmentTopicalREMEDYREPACK INC.70518-1808
mupirocinMupirocin 20 mg/gOintmentTopicalBryant Ranch Prepack71335-2829
mupirocinMupirocin 20 mg/gOintmentTopicalBryant Ranch Prepack72162-2270
mupirocinMupirocin 20 mg/gOintmentTopicalAsclemed USA, Inc.76420-128
Mupirocinmupirocin ointmentMupirocin 20 mg/gOintmentTopicalKesin Pharma Corporation81033-032
mupirocinMupirocin 20 mg/gOintmentTopicalHAWAII REPACK, INC.85534-0038

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