NDC codes

FDA NDC Directory
Product NDC (as listed)73542-101Labeler and product segments. Claims need a package NDC.
Product NDC at billing width73542-0101Add 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
73542-101-25735420101257354201012525 VIAL in 1 CARTON (73542-101-25) / 2 mL in 1 VIALMarketed from Jun 16, 2025

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)
Furosemide
Generic name (nonproprietary)
furosemide
Active ingredients
Furosemide — 10 mg/mL
Dosage form
Injection
Route
Intravenous
Labeler
Maiva Pharma Private LimitedNDC labeler code 73542
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 203428
Marketing start
Listing expires
Other FDA classes
Increased Diuresis at Loop of Henle (Physiologic effect)
Identifiers
Product ID 73542-101_dddc74d0-e63a-431b-a222-12c45bdc0c16SPL ID dddc74d0-e63a-431b-a222-12c45bdc0c16SPL set ID e5880bf4-5037-4813-b7cc-656a6832ecb5RxCUI 1719286, 1719290, 1719291UNII 7LXU5N7ZO5
Pharmacologic class
Loop Diuretic

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

Administration

Drug administration (CPT 96360–96549)

When a clinician administers the drug, the administration is reported separately. Codes in this range cover hydration, therapeutic injections and infusions, and chemotherapy or other complex drug administration. The right code depends on route, duration and drug type, and self-administered drugs are not billed this way.

How CPT relates to drug billing

NDC on a medical claim

N473542010125 followed by a unit qualifier and the quantity

Package 73542-0101-25. 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 .

Full label on DailyMed (opens in a new tab)

About NDC 73542-101

What is NDC 73542-101?
73542-101 is the product NDC for Furosemide, Furosemide 10 mg/mL injection, listed with the FDA by Maiva Pharma Private Limited. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Furosemide.
What is the active ingredient?
Furosemide.
Who is the labeler?
Maiva Pharma Private Limited, NDC labeler code 73542. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Furosemide?
204 other product NDCs are listed under this name. See all Furosemide 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 Furosemide NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
FurosemideFurosemide 10 mg/mLInjectionIntramuscular, IntravenousCivica, Inc.72572-27572572-0275-10
FurosemideFurosemide 20 mg/1TabletOralREMEDYREPACK INC.70518-467970518-4679-00
FurosemideFurosemide 20 mg/1TabletOralUnit Dose Solutions, Inc.87441-03387441-0033-01
FurosemideFurosemide 20 mg/1TabletOralCoupler LLC67046-076867046-0768-03
FurosemideFurosemide 40 mg/1TabletOralREMEDYREPACK INC.70518-460970518-4609-00
FurosemideFurosemide 40 mg/1TabletOralCoupler LLC67046-166367046-1663-03
FurosemideFurosemide 20 mg/1TabletOralMarlex Pharmaceuticals, Inc.10135-83210135-0832-0110135-0832-1010135-0832-90
FurosemideFurosemide 40 mg/1TabletOralMarlex Pharmaceuticals, Inc.10135-83310135-0833-0110135-0833-1010135-0833-90
FurosemideFurosemide 80 mg/1TabletOralMarlex Pharmaceuticals, Inc.10135-83410135-0834-0110135-0834-0510135-0834-90
FurosemideFurosemide 20 mg/1TabletOralGranulation Technology, Inc.63561-016463561-0164-0163561-0164-0263561-0164-09

All 205 Furosemide NDCs

Other NDCs under ANDA 203428

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

FDA NDC Directory listings under ANDA 203428
ProductStrengthForm · routeLabelerProduct NDC
FurosemideFurosemide 10 mg/mLInjection, SolutionIntravenousHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-473
FurosemideFurosemide 10 mg/mLInjection, SolutionIntravenousMedical Purchasing Solutions, LLC71872-7295
FurosemideFurosemide 10 mg/mLInjection, SolutionIntravenousMedical Purchasing Solutions, LLC71872-7308
FurosemideFurosemide 10 mg/mLInjection, SolutionIntravenousMedical Purchasing Solutions, LLC71872-7314
FurosemideFurosemide 10 mg/mLInjection, SolutionIntravenousNorthStar Rx LLC72603-133
FurosemideFurosemide 10 mg/mLInjection, SolutionIntravenousNorthStar Rx LLC72603-251
FurosemideFurosemide 10 mg/mLInjection, SolutionIntravenousNorthStar Rx LLC72603-474
FurosemideFurosemide 10 mg/mLInjectionIntravenousMaiva Pharma Private Limited73542-102
FurosemideFurosemide 10 mg/mLInjectionIntravenousMaiva Pharma Private Limited73542-103
FurosemideFurosemide 10 mg/mLInjection, SolutionIntramuscular, IntravenousAvenacy Inc.83634-302
FurosemideFurosemide 10 mg/mLInjection, SolutionIntravenousProPharma Distribution84549-251
FurosemideFurosemide 10 mg/mLInjection, SolutionIntravenousProPharma Distribution84549-474

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