NDC codes

FDA NDC Directory
Product NDC (as listed)43353-069Labeler and product segments. Claims need a package NDC.
Product NDC at billing width43353-0069Add 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
43353-069-304335300693030 TABLET in 1 BOTTLE (43353-069-30)Marketed from Jun 19, 2017
43353-069-454335300694545 TABLET in 1 BOTTLE (43353-069-45)Marketed from Jun 19, 2017
43353-069-534335300695360 TABLET in 1 BOTTLE (43353-069-53)Marketed from Jun 19, 2017
43353-069-604335300696090 TABLET in 1 BOTTLE (43353-069-60)Marketed from Jun 19, 2017
43353-069-8043353006980180 TABLET in 1 BOTTLE (43353-069-80)Marketed from Jun 19, 2017

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
NDA — New Drug ApplicationApplication NDA 018823
Marketing start
Listing expires
Other FDA classes
Increased Diuresis at Loop of Henle (Physiologic effect)
Identifiers
Product ID 43353-069_13d5f0a8-f822-4190-99b3-32f2a1126cafSPL ID 13d5f0a8-f822-4190-99b3-32f2a1126cafSPL set ID 6fbf7f3d-7566-44d5-9507-c4460238fc91RxCUI 310429, 313988UNII 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 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

N443353006930 followed by a unit qualifier and the quantity

Package 43353-0069-30. 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 is 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 Oral furosemide 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 NDA 018823

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

FDA NDC Directory listings under NDA 018823
ProductStrengthForm · routeLabelerProduct NDC
FurosemideFurosemide 20 mg/1TabletOralNorthwind Health Company, LLC51655-481
FurosemideFurosemide 40 mg/1TabletOralHikma Pharmaceuticals USA Inc.0054-4299
FurosemideFurosemide 20 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC43353-747
FurosemideFurosemide 20 mg/1TabletOralHikma Pharmaceuticals USA Inc.0054-8297
FurosemideFurosemide 20 mg/1TabletOralA-S Medication Solutions50090-6219
FurosemideFurosemide 40 mg/1TabletOralHikma Pharmaceuticals USA Inc.0054-8299
FurosemideFurosemide 20 mg/1TabletOralHikma Pharmaceuticals USA Inc.0054-4297

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