NDC codes

FDA NDC Directory
Product NDC (as listed)70518-4486Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-4486Add 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
70518-4486-07051844860030 TABLET in 1 BLISTER PACK (70518-4486-0)Marketed from Sep 29, 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 — 2 mg/1
Dosage form
Tablet
Route
Oral
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 70518-4486_5b717a1c-5fa8-691f-e063-6394a90a1391SPL ID 5b717a1c-5fa8-691f-e063-6394a90a1391
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

N470518448600 followed by a unit qualifier and the quantity

Package 70518-4486-00. 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.

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/1TabletOralBryant Ranch Prepack71335-2561
GlimepirideGlimepiride 2 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8728
GlimepirideGlimepiride 2 mg/1TabletOralBryant Ranch Prepack71335-2367
GlimepirideGlimepiride 4 mg/1TabletOralREMEDYREPACK INC.70518-4485
GlimepirideGlimepiride 2 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-3639
GlimepirideGlimepiride 4 mg/1TabletOralA-S Medication Solutions50090-7406
GlimepirideGlimepiride 4 mg/1TabletOralA-S Medication Solutions50090-7407
GlimepirideGlimepiride 4 mg/1TabletOralBryant Ranch Prepack71335-2409
GlimepirideGlimepiride 1 mg/1TabletOralA-S Medication Solutions50090-7187
GlimepirideGlimepiride 4 mg/1TabletOralST. MARY'S MEDICAL PARK PHARMACY60760-845
GlimepirideGlimepiride 2 mg/1TabletOralFlorida Pharmaceutical Products, LLC71921-215
GlimepirideGlimepiride 2 mg/1TabletOralCoupler LLC67046-1608
GlimepirideGlimepiride 1 mg/1TabletOralFlorida Pharmaceutical Products, LLC71921-214
GlimepirideGlimepiride 4 mg/1TabletOralFlorida Pharmaceutical Products, LLC71921-216
GlimepirideGlimepiride 2 mg/1TabletOralA-S Medication Solutions50090-7247
GlimepirideGlimepiride 2 mg/1TabletOralA-S Medication Solutions50090-7246
GlimepirideGlimepiride 4 mg/1TabletOralDirect_rx72189-585

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Glimepiride NDC 70518-4486 | Med-Code