NDC codes

FDA NDC Directory
Product NDC (as listed)70518-3774Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-3774Add 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
70518-3774-070518377400705183774001 TUBE in 1 CARTON (70518-3774-0) / 30 g in 1 TUBEMarketed from Jun 22, 2023

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 calcium
Active ingredients
Mupirocin calcium — 20 mg/g
Dosage form
Cream
Route
Topical
Labeler
REMEDYREPACK INC.NDC labeler code 70518
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 207116
Marketing start
Listing expires
Other FDA classes
RNA Synthetase Inhibitors (Mechanism)
Identifiers
Product ID 70518-3774_53843ffd-eba8-d901-e063-6394a90af091SPL ID 53843ffd-eba8-d901-e063-6394a90af091SPL set ID 9a1be092-6fe8-4b7c-a668-e584783f888bRxCUI 311877UNII RG38I2P540
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

N470518377400 followed by a unit qualifier and the quantity

Package 70518-3774-00. 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 Cream USP, 2% is indicated for the treatment of secondarily infected traumatic skin lesions (up to 10 cm in length or 100 cm 2 in area) due to susceptible isolates of Staphylococcus aureus (S. aureus) and Streptococcus pyogenes (S. pyogenes) . Mupirocin cream is an RNA synthetase inhibitor antibacterial indicated for the treatment of secondarily infected traumatic skin lesions (up to 10 cm in length or 100 cm2 in area) 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 70518-3774

What is NDC 70518-3774?
70518-3774 is the product NDC for Mupirocin (mupirocin calcium), Mupirocin calcium 20 mg/g cream, listed with the FDA by REMEDYREPACK INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Mupirocin (Mupirocin Calcium).
What is the active ingredient?
Mupirocin calcium.
Who is the labeler?
REMEDYREPACK INC., NDC labeler code 70518. 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/gOintmentTopicalSt. Mary's Medical Park Pharmacy60760-96060760-0960-22
mupirocinMupirocin 20 mg/gOintmentTopicalPreferred Pharmaceuticals Inc.68788-864268788-8642-02
MupirocinMupirocin 20 mg/gOintmentTopicalPreferred Pharmaceuticals Inc.68788-853468788-8534-02

All 43 Mupirocin NDCs

Other NDCs under ANDA 207116

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

FDA NDC Directory listings under ANDA 207116
ProductStrengthForm · routeLabelerProduct NDC
Mupirocinmupirocin calciumMupirocin calcium 20 mg/gCreamTopicalNORTHSTAR RX LLC16714-055
Mupirocinmupirocin calciumMupirocin calcium 20 mg/gCreamTopicalSun Pharmaceutical Industries, Inc.51672-1370

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