What is NDC 63187-641?

63187-641 is the product NDC for Glimepiride, Glimepiride 2 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 3 package NDCs, shown above in 10- and 11-digit form.

Proficient Rx LP, NDC labeler code 63187. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Glimepiride NDC 63187-641 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)63187-641Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63187-0641Add 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 NDC	11-digit (billing)	Package
63187-641-30	63187064130	30 TABLET in 1 BOTTLE (63187-641-30)Marketed from Dec 1, 2018
63187-641-60	63187064160	60 TABLET in 1 BOTTLE (63187-641-60)Marketed from Dec 1, 2018
63187-641-90	63187064190	90 TABLET in 1 BOTTLE (63187-641-90)Marketed from Dec 1, 2018

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: Proficient Rx LPNDC labeler code 63187
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078181
Marketing start: Aug 23, 2007
Listing expires: Dec 31, 2026
Other FDA classes: Sulfonylurea Compounds (Chemical structure)
Identifiers: Product ID 63187-641_539f397e-9afb-444a-ac5b-c26f4bd791baSPL ID 539f397e-9afb-444a-ac5b-c26f4bd791baSPL set ID beb0cefb-807b-4cc3-ada2-7a8ed4aa8f2bRxCUI 199246UNII 6KY687524KUPC 0363187641306
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

N463187064130 followed by a unit qualifier and the quantity

Package 63187-0641-30. 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 Oct 1, 2022.

Indications (excerpt from the label)

Glimepiride tablets USP 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 )]. Glimepiride is a sulfonylurea indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus ( 1.1 ) Important Limitations of Use: • Not for treating type 1 diabetes mellitus or diabetic ketoacidosis ( 1.1 ) 1.1 Important Limitations of Use Glimepiride tablets USP should not be used for the treatment of type 1 diabetes mellitus or diabetic ketoacidosis, as it would not be effective in these settings.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63187-641

What is NDC 63187-641?: 63187-641 is the product NDC for Glimepiride, Glimepiride 2 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 3 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?: Proficient Rx LP, NDC labeler code 63187. 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Glimepiride	Glimepiride 4 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4191	68788-4191-0368788-4191-0668788-4191-09
Glimepiride	Glimepiride 2 mg/1	TabletOral	Coupler LLC	67046-1608	67046-1608-03
Glimepiride	Glimepiride 2 mg/1	TabletOral	REMEDYREPACK INC.	70518-4486	70518-4486-00
Glimepiride	Glimepiride 4 mg/1	TabletOral	REMEDYREPACK INC.	70518-4485	70518-4485-0070518-4485-0170518-4485-02
Glimepiride	Glimepiride 4 mg/1	TabletOral	Direct_rx	72189-585	72189-0585-90
Glimepiride	Glimepiride 2 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8728	68788-8728-0168788-8728-0368788-8728-06+1 more
Glimepiride	Glimepiride 2 mg/1	TabletOral	Northwind Health Company, LLC	82868-042	82868-0042-90
Glimepiride	Glimepiride 1 mg/1	TabletOral	BluePoint Laboratories	68001-584	68001-0584-0068001-0584-03
Glimepiride	Glimepiride 2 mg/1	TabletOral	BluePoint Laboratories	68001-585	68001-0585-0068001-0585-03
Glimepiride	Glimepiride 4 mg/1	TabletOral	BluePoint Laboratories	68001-586	68001-0586-0068001-0586-03

All 103 Glimepiride NDCs

Other NDCs under ANDA 078181

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

FDA NDC Directory listings under ANDA 078181
Product	Strength	Form · route	Labeler	Product NDC
Glimepiride	Glimepiride 1 mg/1	TabletOral	Proficient Rx LP	63187-698
Glimepiride	Glimepiride 2 mg/1	TabletOral	Bryant Ranch Prepack	71335-0484
Glimepiride	Glimepiride 4 mg/1	TabletOral	Northwind Health Company, LLC	51655-120
Glimepiride	Glimepiride 4 mg/1	TabletOral	Proficient Rx LP	63187-486
Glimepiride	Glimepiride 4 mg/1	TabletOral	Accord Healthcare Inc	16729-003
Glimepiride	Glimepiride 1 mg/1	TabletOral	Accord Healthcare Inc	16729-001
Glimepiride	Glimepiride 2 mg/1	TabletOral	Accord Healthcare Inc	16729-002
Glimepiride	Glimepiride 4 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	43063-587
Glimepiride	Glimepiride 4 mg/1	TabletOral	Bryant Ranch Prepack	71335-0180
Glimepiride	Glimepiride 2 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	43063-630
Glimepiride	Glimepiride 2 mg/1	TabletOral	Northwind Health Company, LLC	51655-383