Prescription drug · ANDA

Amoxicillin NDC 70518-4522

Amoxicillin 400 mg/5mL · Powder, For suspension · Oral · REMEDYREPACK INC.

NDC codes

FDA NDC Directory
Product NDC (as listed)70518-4522Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-4522Add 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
70518-4522-07051845220070518452200100 mL in 1 BOTTLE (70518-4522-0)Marketed from Nov 25, 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)
Amoxicillin
Generic name (nonproprietary)
amoxicillin
Active ingredients
Amoxicillin — 400 mg/5mL
Dosage form
Powder, For suspension
Route
Oral
Labeler
REMEDYREPACK INC.NDC labeler code 70518
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 065334
Marketing start
Listing expires
Other FDA classes
Penicillins (Chemical structure)
Identifiers
Product ID 70518-4522_5b89a37c-c3da-a68e-e063-6294a90a34c1SPL ID 5b89a37c-c3da-a68e-e063-6294a90a34c1

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

N470518452200 followed by a unit qualifier and the quantity

Package 70518-4522-00. 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 70518-4522

What is NDC 70518-4522?
70518-4522 is the product NDC for Amoxicillin, Amoxicillin 400 mg/5mL powder, for suspension, listed with the FDA by REMEDYREPACK INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Amoxicillin.
What is the active ingredient?
Amoxicillin.
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 Amoxicillin?
274 other product NDCs are listed under this name. See all Amoxicillin 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 Amoxicillin NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
AmoxicillinAmoxicillin 250 mg/1CapsuleOralNorthwind Health Company, LLC82868-08882868-0088-30
AmoxicillinAmoxicillin 875 mg/1Tablet, Film coatedOralCoupler LLC67046-073467046-0734-03
AmoxicillinAmoxicillin 875 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-415268788-4152-02
AmoxicillinAmoxicillin 500 mg/1CapsuleOralCoupler LLC67046-031667046-0316-03
AmoxicillinAmoxicillin 250 mg/1CapsuleOralCoupler LLC67046-012767046-0127-03
AmoxicillinAmoxicillin 875 mg/1Tablet, Film coatedOralCoupler LLC67046-001567046-0015-03
AmoxicillinAmoxicillin 500 mg/1CapsuleOralCoupler LLC67046-117567046-1175-03
AmoxicillinAmoxicillin 875 mg/1Tablet, CoatedOralPreferred Pharmaceuticals Inc.68788-406268788-4062-02
AmoxicillinAmoxicillin 400 mg/5mLFor suspensionOralREMEDYREPACK INC.70518-452970518-4529-00
AmoxicillinAmoxicillin 400 mg/5mLPowder, For suspensionOralREMEDYREPACK INC.70518-452170518-4521-00

All 275 Amoxicillin NDCs

Other NDCs under ANDA 065334

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

FDA NDC Directory listings under ANDA 065334
ProductStrengthForm · routeLabelerProduct NDC
AmoxicillinAmoxicillin 400 mg/5mLPowder, For suspensionOralA-S Medication Solutions50090-6323
AmoxicillinAmoxicillin 400 mg/5mLPowder, For suspensionOralA-S Medication Solutions50090-6355
AmoxicillinAmoxicillin 400 mg/5mLPowder, For suspensionOralA-S Medication Solutions50090-6680
AmoxicillinAmoxicillin 200 mg/5mLPowder, For suspensionOralRising Pharma Holdings, Inc.57237-032
AmoxicillinAmoxicillin 400 mg/5mLPowder, For suspensionOralRising Pharma Holdings, Inc.57237-033
AmoxicillinAmoxicillin 400 mg/5mLPowder, For suspensionOralDIRECT RX61919-401
AmoxicillinAmoxicillin 400 mg/5mLPowder, For suspensionOralProficient Rx LP63187-262
AmoxicillinAmoxicillin 400 mg/5mLPowder, For suspensionOralProficient Rx LP63187-335
AmoxicillinAmoxicillin 200 mg/5mLPowder, For suspensionOralAurobindo Pharma Limited65862-070
AmoxicillinAmoxicillin 400 mg/5mLPowder, For suspensionOralAurobindo Pharma Limited65862-071
AmoxicillinAmoxicillin 400 mg/5mLPowder, For suspensionOralNuCare Pharmaceuticals,Inc.68071-5109
AmoxicillinAmoxicillin 200 mg/5mLPowder, For suspensionOralPreferred Pharmaceuticals Inc.68788-8324
AmoxicillinAmoxicillin 400 mg/5mLPowder, For suspensionOralPreferred Pharmaceuticals Inc.68788-8325
AmoxicillinAmoxicillin 200 mg/5mLPowder, For suspensionOralProficient Rx LP71205-775
AmoxicillinAmoxicillin 400 mg/5mLPowder, For suspensionOralDirectRx72189-285

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