NDC codes

FDA NDC Directory
Product NDC (as listed)50090-8144Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-8144Add 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
50090-8144-050090814400500908144001 BOTTLE in 1 CARTON (50090-8144-0) / 30 mL in 1 BOTTLEMarketed from Oct 8, 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)
Azithromycin
Generic name (nonproprietary)
azithromycin
Active ingredients
Azithromycin dihydrate — 200 mg/5mL
Dosage form
Powder, For suspension
Route
Oral
Labeler
A-S Medication SolutionsNDC labeler code 50090
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 217036
Marketing start
Listing expires
Other FDA classes
Macrolides (Chemical structure)
Identifiers
Product ID 50090-8144_02dc1e4a-d2fa-4017-8f6b-64c302d0f103SPL ID 02dc1e4a-d2fa-4017-8f6b-64c302d0f103
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

N450090814400 followed by a unit qualifier and the quantity

Package 50090-8144-00. 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.

About NDC 50090-8144

What is NDC 50090-8144?
50090-8144 is the product NDC for Azithromycin, Azithromycin dihydrate 200 mg/5mL powder, for suspension, listed with the FDA by A-S Medication Solutions. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Azithromycin.
What is the active ingredient?
Azithromycin dihydrate.
Who is the labeler?
A-S Medication Solutions, NDC labeler code 50090. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Azithromycin?
141 other product NDCs are listed under this name. See all Azithromycin 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 Azithromycin NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
azithromycinAzithromycin dihydrate 500 mg/1Tablet, Film coatedOralRising Pharma Holdings, Inc.64980-72664980-0726-0364980-0726-13
azithromycinAzithromycin dihydrate 250 mg/1Tablet, Film coatedOralRising Pharma Holdings, Inc.64980-72764980-0727-0364980-0727-16
azithromycinAzithromycin dihydrate 250 mg/1Tablet, Film coatedOralCoupler LLC67046-050867046-0508-03
AzithromycinAzithromycin dihydrate 100 mg/5mLPowder, For suspensionOralAiPing Pharmaceutical, Inc.11788-12811788-0128-13
AzithromycinAzithromycin dihydrate 200 mg/5mLPowder, For suspensionOralAiPing Pharmaceutical, Inc.11788-12911788-0129-1311788-0129-1411788-0129-15
azithromycinAzithromycin dihydrate 500 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-436770518-4367-0070518-4367-0170518-4367-03+1 more
azithromycinAzithromycin dihydrate 250 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-435670518-4356-00
AzithromycinAzithromycin monohydrate 200 mg/5mLPowder, For suspensionOralPURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS24658-70724658-0707-33
AzithromycinAzithromycin dihydrate 200 mg/5mLPowder, For suspensionOralZhejiang Poly Pharm. Co., Ltd.72673-08172673-0081-60
AzithromycinAzithromycin dihydrate 200 mg/5mLPowder, For suspensionOralZhejiang Poly Pharm. Co., Ltd.72673-08272673-0082-90

All 142 Azithromycin NDCs

Other NDCs under ANDA 217036

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

FDA NDC Directory listings under ANDA 217036
ProductStrengthForm · routeLabelerProduct NDC
AzithromycinAzithromycin dihydrate 100 mg/5mLPowder, For suspensionOralAiPing Pharmaceutical, Inc.11788-128
AzithromycinAzithromycin dihydrate 200 mg/5mLPowder, For suspensionOralAiPing Pharmaceutical, Inc.11788-129
AzithromycinAzithromycin dihydrate 200 mg/5mLPowder, For suspensionOralZhejiang Poly Pharm. Co., Ltd.72673-081
AzithromycinAzithromycin dihydrate 200 mg/5mLPowder, For suspensionOralZhejiang Poly Pharm. Co., Ltd.72673-082
AzithromycinAzithromycin dihydrate 200 mg/5mLPowder, For suspensionOralZhejiang Poly Pharm. Co., Ltd.72673-083
AzithromycinAzithromycin dihydrate 100 mg/5mLPowder, For suspensionOralZhejiang Poly Pharm. Co., Ltd.72673-084
azithromycin dihydrateAzithromycin dihydrate 100 mg/5mLPowder, For suspensionOralSlate Run Pharmaceuticals, LLC70436-220
azithromycin dihydrateAzithromycin dihydrate 200 mg/5mLPowder, For suspensionOralSlate Run Pharmaceuticals, LLC70436-221
azithromycin dihydrateAzithromycin dihydrate 200 mg/5mLPowder, For suspensionOralSlate Run Pharmaceuticals, LLC70436-222
azithromycin dihydrateAzithromycin dihydrate 200 mg/5mLPowder, For suspensionOralSlate Run Pharmaceuticals, LLC70436-228

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