NDC codes

FDA NDC Directory
Product NDC (as listed)83980-003Labeler and product segments. Claims need a package NDC.
Product NDC at billing width83980-0003Add 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
83980-003-0183980000301100 TABLET in 1 BOTTLE (83980-003-01)Marketed from Jun 3, 2024
83980-003-10839800003101000 TABLET in 1 BOTTLE (83980-003-10)Marketed from Jun 3, 2024
83980-003-978398000039710 TABLET in 1 BOTTLE (83980-003-97)Marketed from Jun 3, 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)
Furosemide
Generic name (nonproprietary)
furosemide
Active ingredients
Furosemide — 40 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 078010
Marketing start
Listing expires
Other FDA classes
Increased Diuresis at Loop of Henle (Physiologic effect)
Identifiers
Product ID 83980-003_2ef79eb1-61e5-4697-9292-336ca5cf5116SPL ID 2ef79eb1-61e5-4697-9292-336ca5cf5116SPL set ID 0acd293b-ecab-4879-a8e7-cd1b76148f2aRxCUI 197732, 310429, 313988UNII 7LXU5N7ZO5UPC 0383980004016, 0383980003019, 0383980002012
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 HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N483980000301 followed by a unit qualifier and the quantity

Package 83980-0003-01. 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)

INDICATIONS AND USAGE Edema Furosemide tablets are indicated in adults and pediatric patients for the treatment of edema associated with congestive heart failure, cirrhosis of the liver, and renal disease, including the nephrotic syndrome. Furosemide is particularly useful when an agent with greater diuretic potential is desired. Hypertension Furosemide tablets may be used in adults for the treatment of hypertension alone or in combination with other antihypertensive agents. Hypertensive patients who cannot be adequately controlled with thiazides will probably also not be adequately controlled with furosemide alone.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 078010

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

FDA NDC Directory listings under ANDA 078010
ProductStrengthForm · routeLabelerProduct NDC
FurosemideFurosemide 20 mg/1TabletOralA-S Medication Solutions50090-7706
FurosemideFurosemide 40 mg/1TabletOralA-S Medication Solutions50090-7703
FurosemideFurosemide 40 mg/1TabletOralA-S Medication Solutions50090-7704
FurosemideFurosemide 40 mg/1TabletOralA-S Medication Solutions50090-7705
FurosemideFurosemide 20 mg/1TabletOralA-S Medication Solutions50090-7708
FurosemideFurosemide 20 mg/1TabletOralIpca Laboratories Limited83980-002
FurosemideFurosemide 80 mg/1TabletOralIpca Laboratories Limited83980-004
FurosemideFurosemide 20 mg/1TabletOralCoupler LLC67046-1589
FurosemideFurosemide 40 mg/1TabletOralCoupler LLC67046-1663
FurosemideFurosemide 20 mg/1TabletOralREMEDYREPACK INC.70518-4679

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