NDC codes

FDA NDC Directory
Product NDC (as listed)68788-4073Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68788-4073Add 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
68788-4073-16878840730168788407301100 TABLET in 1 BOTTLE (68788-4073-1)Marketed from Jan 27, 2026
68788-4073-3687884073036878840730330 TABLET in 1 BOTTLE (68788-4073-3)Marketed from Jan 27, 2026
68788-4073-6687884073066878840730660 TABLET in 1 BOTTLE (68788-4073-6)Marketed from Jan 27, 2026
68788-4073-9687884073096878840730990 TABLET in 1 BOTTLE (68788-4073-9)Marketed from Jan 27, 2026

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
Preferred Pharmaceuticals Inc.NDC labeler code 68788
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 074388
Marketing start
Listing expires
Other FDA classes
Sulfonylurea Compounds (Chemical structure)
Identifiers
Product ID 68788-4073_bc8df889-25e0-49a0-bbec-a3dfae8bbb8aSPL ID bc8df889-25e0-49a0-bbec-a3dfae8bbb8aSPL set ID bc8df889-25e0-49a0-bbec-a3dfae8bbb8aRxCUI 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

N468788407301 followed by a unit qualifier and the quantity

Package 68788-4073-01. 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)

INDICATIONS AND USAGE Glyburide tablets USP 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 68788-4073

What is NDC 68788-4073?
68788-4073 is the product NDC for Glyburide, Glyburide 5 mg/1 tablet, listed with the FDA by Preferred Pharmaceuticals Inc.. It has 4 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?
Preferred Pharmaceuticals Inc., NDC labeler code 68788. 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 2.5 mg/1TabletOralCoupler LLC67046-162067046-1620-03
GlyburideGlyburide 5 mg/1TabletOralREMEDYREPACK INC.70518-403570518-4035-0070518-4035-01
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 074388

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

FDA NDC Directory listings under ANDA 074388
ProductStrengthForm · routeLabelerProduct NDC
GlyburideGlyburide 1.25 mg/1TabletOralTeva Pharmaceuticals USA, Inc.0093-8342
GlyburideGlyburide 2.5 mg/1TabletOralTeva Pharmaceuticals USA, Inc.0093-8343
GlyburideGlyburide 5 mg/1TabletOralTeva Pharmaceuticals USA, Inc.0093-8344
GlyburideGlyburide 5 mg/1TabletOralA-S Medication Solutions50090-6607
GlyburideGlyburide 2.5 mg/1TabletOralProficient Rx LP63187-848
GlyburideGlyburide 2.5 mg/1TabletOralCoupler LLC67046-1620
GlyburideGlyburide 5 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-3677
GlyburideGlyburide 5 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-3702
GlyburideGlyburide 5 mg/1TabletOralProficient Rx LP82804-150

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