NDC codes

FDA NDC Directory
Product NDC (as listed)60429-919Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60429-0919Add 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
60429-919-0160429091901100 TABLET in 1 BOTTLE (60429-919-01)Marketed from Dec 21, 2016

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)
Glimepiride
Generic name (nonproprietary)
glimepiride
Active ingredients
Glimepiride — 2 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Golden State Medical Supply, Inc.NDC labeler code 60429
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 077911
Marketing start
Listing expires
Other FDA classes
Sulfonylurea Compounds (Chemical structure)
Identifiers
Product ID 60429-919_288c1f6b-3779-3b65-e063-6394a90ae906SPL ID 288c1f6b-3779-3b65-e063-6394a90ae906SPL set ID 4f83e203-c102-47fa-bb8e-4fc5541e0d6fRxCUI 199245, 199246, 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

N460429091901 followed by a unit qualifier and the quantity

Package 60429-0919-01. 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)

Glimepiride Tablet are indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus [see Clinical Studies ( 14.1 ) ]. Limitations of Use Glimepiride should not be used for the treatment of type 1 diabetes mellitus or diabetic ketoacidosis, as it would not be effective in these settings. Glimepiride Tablets are a sulfonylurea indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus ( 1 ). Important Limitations of Use: Not for treating type 1 diabetes mellitus or diabetic ketoacidosis ( 1 ).

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 60429-919

What is NDC 60429-919?
60429-919 is the product NDC for Glimepiride, Glimepiride 2 mg/1 tablet, listed with the FDA by Golden State Medical Supply, Inc.. It has 1 package NDC, 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?
Golden State Medical Supply, Inc., NDC labeler code 60429. 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?
102 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 103 Glimepiride NDCs

Other NDCs under ANDA 077911

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

FDA NDC Directory listings under ANDA 077911
ProductStrengthForm · routeLabelerProduct NDC
GlimepirideGlimepiride 2 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.43063-698
GlimepirideGlimepiride 4 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.43063-699
GlimepirideGlimepiride 4 mg/1TabletOralCarlsbad Technology, Inc.61442-117
GlimepirideGlimepiride 1 mg/1TabletOralCarlsbad Technology, Inc.61442-115
GlimepirideGlimepiride 2 mg/1TabletOralCarlsbad Technology, Inc.61442-116
GlimepirideGlimepiride 2 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.43063-946
GlimepirideGlimepiride 4 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-048
GlimepirideGlimepiride 1 mg/1TabletOralGolden State Medical Supply, Inc.60429-918
GlimepirideGlimepiride 4 mg/1TabletOralGolden State Medical Supply, Inc.60429-920
GlimepirideGlimepiride 4 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-236
GlimepirideGlimepiride 1 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.43063-697

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