NDC codes

FDA NDC Directory
Product NDC (as listed)70518-4485Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-4485Add 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
70518-4485-07051844850070518448500100 TABLET in 1 BOTTLE, PLASTIC (70518-4485-0)Marketed from Sep 28, 2025
70518-4485-1705184485017051844850190 TABLET in 1 BOTTLE, PLASTIC (70518-4485-1)Marketed from Oct 3, 2025
70518-4485-2705184485027051844850230 TABLET in 1 BLISTER PACK (70518-4485-2)Marketed from Nov 5, 2025

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
REMEDYREPACK INC.NDC labeler code 70518
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 202112
Marketing start
Listing expires
Other FDA classes
Sulfonylurea Compounds (Chemical structure)
Identifiers
Product ID 70518-4485_5b3acede-23f5-2527-e063-6294a90a3a99SPL ID 5b3acede-23f5-2527-e063-6294a90a3a99
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

N470518448500 followed by a unit qualifier and the quantity

Package 70518-4485-00. 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 70518-4485

What is NDC 70518-4485?
70518-4485 is the product NDC for Glimepiride, Glimepiride 4 mg/1 tablet, listed with the FDA by REMEDYREPACK INC.. 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?
REMEDYREPACK INC., NDC labeler code 70518. 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/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
GlimepirideGlimepiride 1 mg/1TabletOralA-S Medication Solutions50090-718750090-7187-0050090-7187-0150090-7187-02

All 102 Glimepiride NDCs

Other NDCs under ANDA 202112

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

FDA NDC Directory listings under ANDA 202112
ProductStrengthForm · routeLabelerProduct NDC
GlimepirideGlimepiride 1 mg/1TabletOralA-S Medication Solutions50090-7187
GlimepirideGlimepiride 2 mg/1TabletOralA-S Medication Solutions50090-7246
GlimepirideGlimepiride 2 mg/1TabletOralA-S Medication Solutions50090-7247
GlimepirideGlimepiride 4 mg/1TabletOralA-S Medication Solutions50090-7406
GlimepirideGlimepiride 4 mg/1TabletOralA-S Medication Solutions50090-7407
GlimepirideGlimepiride 4 mg/1TabletOralST. MARY'S MEDICAL PARK PHARMACY60760-845
GlimepirideGlimepiride 2 mg/1TabletOralCoupler LLC67046-1608
GlimepirideGlimepiride 2 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-3639
GlimepirideGlimepiride 4 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-4191
GlimepirideGlimepiride 2 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8728
GlimepirideGlimepiride 2 mg/1TabletOralREMEDYREPACK INC.70518-4486
GlimepirideGlimepiride 2 mg/1TabletOralBryant Ranch Prepack71335-2367
GlimepirideGlimepiride 4 mg/1TabletOralBryant Ranch Prepack71335-2409
GlimepirideGlimepiride 1 mg/1TabletOralBryant Ranch Prepack71335-2561
GlimepirideGlimepiride 1 mg/1TabletOralFlorida Pharmaceutical Products, LLC71921-214
GlimepirideGlimepiride 2 mg/1TabletOralFlorida Pharmaceutical Products, LLC71921-215
GlimepirideGlimepiride 4 mg/1TabletOralFlorida Pharmaceutical Products, LLC71921-216
GlimepirideGlimepiride 4 mg/1TabletOralDirect_rx72189-585

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