NDC codes

FDA NDC Directory
Product NDC (as listed)50090-6937Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-6937Add 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
50090-6937-05009069370090 TABLET in 1 BOTTLE (50090-6937-0)Marketed from Dec 15, 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)
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 077293
Marketing start
Listing expires
Other FDA classes
Increased Diuresis at Loop of Henle (Physiologic effect)
Identifiers
Product ID 50090-6937_f1e4d5a1-fc65-47ce-b6bd-47b1c793dccfSPL ID f1e4d5a1-fc65-47ce-b6bd-47b1c793dccfSPL set ID 60cf5e60-9a7a-42c2-95b5-016f7a68ffc4RxCUI 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

N450090693700 followed by a unit qualifier and the quantity

Package 50090-6937-00. 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 077293

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

FDA NDC Directory listings under ANDA 077293
ProductStrengthForm · routeLabelerProduct NDC
FurosemideFurosemide 20 mg/1TabletOralBryant Ranch Prepack71335-0384
FurosemideFurosemide 80 mg/1TabletOralLeading Pharma, LLC69315-118
FurosemideFurosemide 40 mg/1TabletOralPreferred Pharmaceuticals, Inc.68788-6784
FurosemideFurosemide 20 mg/1TabletOralCalvin Scott & Co., Inc.17224-178
FurosemideFurosemide 40 mg/1TabletOralCalvin Scott & Co., Inc.17224-185
FurosemideFurosemide 20 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-6948
FurosemideFurosemide 40 mg/1TabletOralNorthwind Health Company, LLC51655-517
FurosemideFurosemide 20 mg/1TabletOralA-S Medication Solutions50090-5429
FurosemideFurosemide 40 mg/1TabletOralA-S Medication Solutions50090-3313
FurosemideFurosemide 40 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-3273
FurosemideFurosemide 20 mg/1TabletOralProficient Rx LP63187-739
FurosemideFurosemide 20 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-843
FurosemideFurosemide 20 mg/1TabletOralDIRECT RX61919-242
FurosemideFurosemide 40 mg/1TabletOralDirect_Rx61919-255
FurosemideFurosemide 80 mg/1TabletOralCoupler LLC67046-1555
FurosemideFurosemide 40 mg/1TabletOralProficient Rx LP63187-790
FurosemideFurosemide 20 mg/1TabletOralCoupler LLC67046-0768
FurosemideFurosemide 20 mg/1TabletOralREMEDYREPACK INC.70518-2528
FurosemideFurosemide 20 mg/1TabletOralNorthwind Health Company, LLC51655-269
FurosemideFurosemide 20 mg/1TabletOralUnit Dose Solutions, Inc.87441-033

Showing 20 of 34.

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free Med-Code account to keep looking up NDCs, J-codes and drugs.

Create a free accountLog in