NDC codes

FDA NDC Directory
Product NDC (as listed)45802-112Labeler and product segments. Claims need a package NDC.
Product NDC at billing width45802-0112Add 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
45802-112-14458020112141 TUBE in 1 CARTON (45802-112-14) / 15 g in 1 TUBEMarketed from Oct 8, 2022
45802-112-22458020112221 TUBE in 1 CARTON (45802-112-22) / 22 g in 1 TUBEMarketed from Oct 30, 2009

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
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 45802-112_d51e7348-2495-41d4-93c1-bfaef2dac375SPL ID d51e7348-2495-41d4-93c1-bfaef2dac375SPL set ID e9b61f01-3c67-42a4-a62b-10f1d1343190RxCUI 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

N445802011214 followed by a unit qualifier and the quantity

Package 45802-0112-14. 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. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

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/gOintmentTopicalProficient Rx LP63187-261
mupirocinMupirocin 20 mg/gOintmentTopicalBryant Ranch Prepack72162-2270
mupirocinMupirocin 20 mg/gOintmentTopicalNuCare Pharmaceuticals,Inc.68071-4789
mupirocinMupirocin 20 mg/gOintmentTopicalPreferred Pharmaceuticals Inc.68788-8642
mupirocinMupirocin 20 mg/gOintmentTopicalBryant Ranch Prepack63629-8687
mupirocinMupirocin 20 mg/gOintmentTopicalATLANTIC BIOLOGICALS CORP.17856-0112
mupirocinMupirocin 20 mg/gOintmentTopicalSt. Mary's Medical Park Pharmacy60760-960
Mupirocinmupirocin ointmentMupirocin 20 mg/gOintmentTopicalKesin Pharma Corporation81033-032
mupirocinMupirocin 20 mg/gOintmentTopicalAsclemed USA, Inc.76420-128
mupirocinMupirocin 20 mg/gOintmentTopicalHAWAII REPACK, INC.85534-0038
mupirocinMupirocin 20 mg/gOintmentTopicalA-S Medication Solutions50090-1587
mupirocinMupirocin 20 mg/gOintmentTopicalBryant Ranch Prepack71335-2829
mupirocinMupirocin 20 mg/gOintmentTopicalREMEDYREPACK INC.70518-1808

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