NDC codes

FDA NDC Directory
Product NDC (as listed)71205-158Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71205-0158Add 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
71205-158-03712050158033 TABLET, FILM COATED in 1 BOTTLE (71205-158-03)Marketed from Nov 1, 2018
71205-158-06712050158066 TABLET, FILM COATED in 1 BOTTLE (71205-158-06)Marketed from Nov 1, 2018
71205-158-307120501583030 TABLET, FILM COATED in 1 BOTTLE (71205-158-30)Marketed from Nov 1, 2018
71205-158-66712050158661 BLISTER PACK in 1 CARTON (71205-158-66) / 6 TABLET, FILM COATED in 1 BLISTER PACKMarketed from Dec 11, 2019

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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)
Azithromycin
Generic name (nonproprietary)
azithromycin
Active ingredients
Azithromycin dihydrate — 250 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 207370
Marketing start
Listing expires
Other FDA classes
Macrolides (Chemical structure)
Identifiers
Product ID 71205-158_d47fa421-e017-48f1-95a9-c0922cca63d6SPL ID d47fa421-e017-48f1-95a9-c0922cca63d6SPL set ID cb40f4cf-15ae-47ab-8e0a-979467fa0d9eRxCUI 308460UNII 5FD1131I7SUPC 0371205158668
Pharmacologic class
Macrolide Antimicrobial

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

N471205015803 followed by a unit qualifier and the quantity

Package 71205-0158-03. 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 207370

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

FDA NDC Directory listings under ANDA 207370
ProductStrengthForm · routeLabelerProduct NDC
AzithromycinAzithromycin dihydrate 250 mg/1Tablet, Film coatedOralDIRECT RX72189-087
AzithromycinAzithromycin dihydrate 250 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-4720
AzithromycinAzithromycin dihydrate 250 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-4721
AzithromycinAzithromycin dihydrate 250 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-8012
AzithromycinAzithromycin dihydrate 250 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-2433
AzithromycinAzithromycin dihydrate 250 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-4812
AzithromycinAzithromycin dihydrate 250 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-4902
AzithromycinAzithromycin dihydrate 250 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-8702
AzithromycinAzithromycin dihydrate 250 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-7550
AzithromycinAzithromycin dihydrate 250 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-2668
AzithromycinAzithromycin dihydrate 250 mg/1Tablet, Film coatedOralAurobindo Pharma Limited65862-641

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