NDC codes

FDA NDC Directory
Product NDC (as listed)70518-4035Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-4035Add 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
70518-4035-0705184035007051840350030 TABLET in 1 BLISTER PACK (70518-4035-0)Marketed from Mar 11, 2024
70518-4035-17051840350170518403501360 TABLET in 1 BOTTLE, PLASTIC (70518-4035-1)Marketed from Jun 24, 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)
Glyburide
Generic name (nonproprietary)
glyburide
Active ingredients
Glyburide — 5 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 203379
Marketing start
Listing expires
Other FDA classes
Sulfonylurea Compounds (Chemical structure)
Identifiers
Product ID 70518-4035_54112e49-0ae5-6ec9-e063-6394a90a3616SPL ID 54112e49-0ae5-6ec9-e063-6394a90a3616SPL set ID 524eec41-37ee-419a-b7a1-d23e888ae6abRxCUI 310537UNII SX6K58TVWC
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

N470518403500 followed by a unit qualifier and the quantity

Package 70518-4035-00. 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

Current FDA label (SPL), effective .

Indications (excerpt from the label)

INDICATIONS & USAGE Glyburide tablets are indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70518-4035

What is NDC 70518-4035?
70518-4035 is the product NDC for Glyburide, Glyburide 5 mg/1 tablet, listed with the FDA by REMEDYREPACK INC.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Glyburide.
What is the active ingredient?
Glyburide.
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 Glyburide?
51 other product NDCs are listed under this name. See all Glyburide 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 Glyburide NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
GlyburideGlyburide 5 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-407368788-4073-0168788-4073-0368788-4073-06+1 more
GlyburideGlyburide 2.5 mg/1TabletOralCoupler LLC67046-162067046-1620-03
GlyburideGlyburide 5 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-850868788-8508-0168788-8508-0368788-8508-06+1 more
GlyburideGlyburide 2.5 mg/1TabletOralREMEDYREPACK INC.70518-350470518-3504-0070518-3504-01
GlyburideGlyburide 5 mg/1TabletOralA-S Medication Solutions50090-619650090-6196-0050090-6196-0150090-6196-02+2 more
GlyburideGlyburide 2.5 mg/1TabletOralA-S Medication Solutions50090-740850090-7408-0050090-7408-02
GlyburideGlyburide 5 mg/1TabletOralA-S Medication Solutions50090-785950090-7859-00
GlyburideGlyburide 5 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-345268071-3452-0368071-3452-06
GlyburideGlyburide 5 mg/1TabletOralBryant Ranch Prepack71335-277171335-2771-0171335-2771-0271335-2771-03+3 more
GlyburideGlyburide 1.25 mg/1TabletOralModavar Pharmaceuticals LLC72241-03872241-0038-0572241-0038-11

All 52 Glyburide NDCs

Other NDCs under ANDA 203379

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

FDA NDC Directory listings under ANDA 203379
ProductStrengthForm · routeLabelerProduct NDC
GlyburideGlyburide 5 mg/1TabletOralA-S Medication Solutions50090-6196
GlyburideGlyburide 2.5 mg/1TabletOralA-S Medication Solutions50090-7408
GlyburideGlyburide 5 mg/1TabletOralA-S Medication Solutions50090-7859
GlyburideGlyburide 5 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-3452
GlyburideGlyburide 5 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8508
GlyburideGlyburide 2.5 mg/1TabletOralREMEDYREPACK INC.70518-3504
GlyburideGlyburide 1.25 mg/1TabletOralCadila Pharmaceuticals Limited71209-009
GlyburideGlyburide 2.5 mg/1TabletOralCadila Pharmaceuticals Limited71209-010
GlyburideGlyburide 5 mg/1TabletOralCadila Pharmaceuticals Limited71209-011
GlyburideGlyburide 5 mg/1TabletOralBryant Ranch Prepack71335-2771
GlyburideGlyburide 1.25 mg/1TabletOralModavar Pharmaceuticals LLC72241-038
GlyburideGlyburide 2.5 mg/1TabletOralModavar Pharmaceuticals LLC72241-039
GlyburideGlyburide 5 mg/1TabletOralModavar Pharmaceuticals LLC72241-040

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