NDC codes

FDA NDC Directory
Product NDC (as listed)50090-5593Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-5593Add 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
50090-5593-05009055930012 TABLET in 1 BOTTLE (50090-5593-0)Marketed from Jul 16, 2021

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)
Acetazolamide
Generic name (nonproprietary)
acetazolamide
Active ingredients
Acetazolamide — 250 mg/1
Dosage form
Tablet
Route
Oral
Labeler
A-S Medication SolutionsNDC labeler code 50090
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 209734
Marketing start
Listing expires
Other FDA classes
Carbonic Anhydrase Inhibitors (Mechanism)Sulfonamides (Chemical structure)
Identifiers
Product ID 50090-5593_3563ed78-d80d-420f-8f75-e776e4f892b6SPL ID 3563ed78-d80d-420f-8f75-e776e4f892b6
Pharmacologic class
Carbonic Anhydrase Inhibitor

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

N450090559300 followed by a unit qualifier and the quantity

Package 50090-5593-00. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 50090-5593

What is NDC 50090-5593?
50090-5593 is the product NDC for Acetazolamide, Acetazolamide 250 mg/1 tablet, listed with the FDA by A-S Medication Solutions. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Acetazolamide.
What is the active ingredient?
Acetazolamide.
Who is the labeler?
A-S Medication Solutions, NDC labeler code 50090. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Acetazolamide?
70 other product NDCs are listed under this name. See all Acetazolamide 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 Acetazolamide NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
AcetazolamideAcetazolamide 500 mg/1Capsule, Extended releaseOralREMEDYREPACK INC.70518-464670518-4646-00
AcetazolamideAcetazolamide 125 mg/1TabletOralMarlex Pharmaceuticals, Inc.10135-83010135-0830-01
AcetazolamideAcetazolamide 250 mg/1TabletOralMarlex Pharmaceuticals, Inc.10135-83110135-0831-01
Acetazolamideacetazolamide sodiumAcetazolamide sodium 500 mg/5mLInjection, Powder, For solutionIntravenousSagent Pharmaceuticals25021-83925021-0839-20
AcetazolamideAcetazolamide sodium 500 mg/5mLInjection, Powder, Lyophilized, For solutionIntravenousGland Pharma Limited68083-66168083-0661-01
AcetazolamideAcetazolamide 250 mg/1TabletOralAurobindo Pharma Limited59651-90659651-0906-01
AcetazolamideAcetazolamide 125 mg/1TabletOralAurobindo Pharma Limited59651-90559651-0905-01
AcetazolamideAcetazolamide 125 mg/1TabletOralAarkish Pharmaceuticals NJ Inc.81005-10481005-0104-0181005-0104-10
AcetazolamideAcetazolamide 250 mg/1TabletOralAarkish Pharmaceuticals NJ Inc.81005-10581005-0105-0181005-0105-10
AcetazolamideAcetazolamide 125 mg/1TabletOralAjanta Pharma USA Inc.27241-13227241-0132-04

All 71 Acetazolamide NDCs

Other NDCs under ANDA 209734

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

FDA NDC Directory listings under ANDA 209734
ProductStrengthForm · routeLabelerProduct NDC
AcetazolamideAcetazolamide 125 mg/1TabletOralProficient Rx LP71205-308
AcetazolamideAcetazolamide 125 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-045
AcetazolamideAcetazolamide 250 mg/1TabletOralAvPAK50268-054
AcetazolamideAcetazolamide 125 mg/1TabletOralStrides Pharma Science Limited64380-833
AcetazolamideAcetazolamide 250 mg/1TabletOralStrides Pharma Science Limited64380-834
AcetazolamideAcetazolamide 125 mg/1TabletOralNuCare Pharmaceuticlas, Inc.68071-3728

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Acetazolamide NDC 50090-5593 | National Drug Code | Med-Code