NDC codes

FDA NDC Directory
Product NDC (as listed)50090-7703Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-7703Add 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
50090-7703-05009077030030 TABLET in 1 BOTTLE (50090-7703-0)Marketed from Oct 14, 2025
50090-7703-150090770301100 TABLET in 1 BOTTLE (50090-7703-1)Marketed from Oct 14, 2025
50090-7703-35009077030360 TABLET in 1 BOTTLE (50090-7703-3)Marketed from Oct 14, 2025
50090-7703-95009077030990 TABLET in 1 BOTTLE (50090-7703-9)Marketed from Oct 14, 2025

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)
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 50090-7703_3c548f50-8fb7-42f1-a142-d0260d00fb08SPL ID 3c548f50-8fb7-42f1-a142-d0260d00fb08SPL set ID 5d7eb469-2371-4abb-8f49-be1596f10f27RxCUI 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

N450090770300 followed by a unit qualifier and the quantity

Package 50090-7703-00. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

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 Solutions50090-7704
FurosemideFurosemide 40 mg/1TabletOralA-S Medication Solutions50090-7705
FurosemideFurosemide 20 mg/1TabletOralA-S Medication Solutions50090-7708
FurosemideFurosemide 20 mg/1TabletOralIpca Laboratories Limited83980-002
FurosemideFurosemide 40 mg/1TabletOralIpca Laboratories Limited83980-003
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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