NDC codes

FDA NDC Directory
Product NDC (as listed)50090-6322Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-6322Add 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
50090-6322-0500906322005009063220030 TABLET in 1 BOTTLE (50090-6322-0)Marketed from Jan 10, 2023
50090-6322-15009063220150090632201100 TABLET in 1 BOTTLE (50090-6322-1)Marketed from Jan 10, 2023
50090-6322-2500906322025009063220260 TABLET in 1 BOTTLE (50090-6322-2)Marketed from Jan 10, 2023
50090-6322-3500906322035009063220390 TABLET in 1 BOTTLE (50090-6322-3)Marketed from Jan 10, 2023
50090-6322-45009063220450090632204180 TABLET in 1 BOTTLE (50090-6322-4)Marketed from Jan 10, 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)
Glimepiride
Generic name (nonproprietary)
glimepiride
Active ingredients
Glimepiride — 4 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 202759
Marketing start
Listing expires
Other FDA classes
Sulfonylurea Compounds (Chemical structure)
Identifiers
Product ID 50090-6322_f6d891ed-a372-4f20-b4d3-a77f3af53d71SPL ID f6d891ed-a372-4f20-b4d3-a77f3af53d71SPL set ID a11680ba-2750-43ab-a1b1-a52ebe3e139fRxCUI 199247UNII 6KY687524K
Pharmacologic class
Sulfonylurea

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

N450090632200 followed by a unit qualifier and the quantity

Package 50090-6322-00. 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.

About NDC 50090-6322

What is NDC 50090-6322?
50090-6322 is the product NDC for Glimepiride, Glimepiride 4 mg/1 tablet, listed with the FDA by A-S Medication Solutions. It has 5 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Glimepiride.
What is the active ingredient?
Glimepiride.
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 Glimepiride?
101 other product NDCs are listed under this name. See all Glimepiride 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 Glimepiride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
GlimepirideGlimepiride 4 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-419168788-4191-0368788-4191-0668788-4191-09
GlimepirideGlimepiride 2 mg/1TabletOralCoupler LLC67046-160867046-1608-03
GlimepirideGlimepiride 2 mg/1TabletOralREMEDYREPACK INC.70518-448670518-4486-00
GlimepirideGlimepiride 4 mg/1TabletOralREMEDYREPACK INC.70518-448570518-4485-0070518-4485-0170518-4485-02
GlimepirideGlimepiride 4 mg/1TabletOralDirect_rx72189-58572189-0585-90
GlimepirideGlimepiride 2 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-872868788-8728-0168788-8728-0368788-8728-06+1 more
GlimepirideGlimepiride 2 mg/1TabletOralNorthwind Health Company, LLC82868-04282868-0042-90
GlimepirideGlimepiride 1 mg/1TabletOralBluePoint Laboratories68001-58468001-0584-0068001-0584-03
GlimepirideGlimepiride 2 mg/1TabletOralBluePoint Laboratories68001-58568001-0585-0068001-0585-03
GlimepirideGlimepiride 4 mg/1TabletOralBluePoint Laboratories68001-58668001-0586-0068001-0586-03

All 102 Glimepiride NDCs

Other NDCs under ANDA 202759

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

FDA NDC Directory listings under ANDA 202759
ProductStrengthForm · routeLabelerProduct NDC
GlimepirideGlimepiride 1 mg/1TabletOralRising Pharma Holdings, Inc.16571-773
GlimepirideGlimepiride 2 mg/1TabletOralRising Pharma Holdings, Inc.16571-774
GlimepirideGlimepiride 4 mg/1TabletOralRising Pharma Holdings, Inc.16571-775
GlimepirideGlimepiride 1 mg/1TabletOralA-S Medication Solutions50090-6394
GlimepirideGlimepiride 2 mg/1TabletOralA-S Medication Solutions50090-6426
GlimepirideGlimepiride 2 mg/1TabletOralA-S Medication Solutions50090-7628
GlimepirideGlimepiride 4 mg/1TabletOralA-S Medication Solutions50090-7823
GlimepirideGlimepiride 4 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-800
GlimepirideGlimepiride 2 mg/1TabletOralAurobindo Pharma Limited65862-580
GlimepirideGlimepiride 4 mg/1TabletOralAurobindo Pharma Limited65862-581
GlimepirideGlimepiride 4 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8432
GlimepirideGlimepiride 4 mg/1TabletOralProficient Rx LP71205-773
GlimepirideGlimepiride 1 mg/1TabletOralProficient Rx LP71205-779
GlimepirideGlimepiride 4 mg/1TabletOralBryant Ranch Prepack71335-9654
GlimepirideGlimepiride 1 mg/1TabletOralBryant Ranch Prepack71335-9655
GlimepirideGlimepiride 2 mg/1TabletOralDirect_Rx72189-485
GlimepirideGlimepiride 2 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-370
GlimepirideGlimepiride 2 mg/1TabletOralProficient Rx LP82804-065
GlimepirideGlimepiride 2 mg/1TabletOralNorthwind Health Company, LLC82868-042

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