NDC codes

FDA NDC Directory
Product NDC (as listed)71335-1886Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-1886Add 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
71335-1886-17133518860130 TABLET in 1 BOTTLE (71335-1886-1)Marketed from Dec 21, 2021
71335-1886-27133518860260 TABLET in 1 BOTTLE (71335-1886-2)Marketed from Dec 21, 2021
71335-1886-37133518860390 TABLET in 1 BOTTLE (71335-1886-3)Marketed from Dec 21, 2021
71335-1886-471335188604100 TABLET in 1 BOTTLE (71335-1886-4)Marketed from Dec 21, 2021
71335-1886-571335188605180 TABLET in 1 BOTTLE (71335-1886-5)Marketed from Dec 21, 2021

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 091220
Marketing start
Listing expires
Other FDA classes
Sulfonylurea Compounds (Chemical structure)
Identifiers
Product ID 71335-1886_6cd6038e-4934-47ee-8590-66e556eefdcbSPL ID 6cd6038e-4934-47ee-8590-66e556eefdcbSPL set ID 62780d2e-083d-4bcb-99ff-1b1b4ade60d9RxCUI 199246UNII 6KY687524K
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

N471335188601 followed by a unit qualifier and the quantity

Package 71335-1886-01. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 091220

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

FDA NDC Directory listings under ANDA 091220
ProductStrengthForm · routeLabelerProduct NDC
Glimepiride 3 mgglimepirideGlimepiride 3 mg/1TabletOralLifsa Drugs LLC72336-641
GlimepirideGlimepiride 1 mg/1TabletOralBryant Ranch Prepack71335-1885
GlimepirideGlimepiride 2 mg/1TabletOralBluePoint Laboratories68001-585
GlimepirideGlimepiride 1 mg/1TabletOralBluePoint Laboratories68001-584
GlimepirideGlimepiride 4 mg/1TabletOralBluePoint Laboratories68001-586
GlimepirideGlimepiride 4 mg/1TabletOralMicro Labs Limited42571-103
GlimepirideGlimepiride 1 mg/1TabletOralMicro Labs Limited42571-100
GlimepirideGlimepiride 2 mg/1TabletOralMicro Labs Limited42571-101
GlimepirideGlimepiride 3 mg/1TabletOralMicro Labs Limited42571-102
GlimepirideGlimepiride 6 mg/1TabletOralMicro Labs Limited42571-104
GlimepirideGlimepiride 8 mg/1TabletOralMicro Labs Limited42571-105
GlimepirideGlimepiride 1 mg/1TabletOralNCS HealthCare of KY, Inc dba Vangard Labs0615-8332
GlimepirideGlimepiride 2 mg/1TabletOralNCS HealthCare of KY, Inc dba Vangard Labs0615-8333
GlimepirideGlimepiride 4 mg/1TabletOralNCS HealthCare of KY, Inc dba Vangard Labs0615-8334

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