What is NDC 62135-089?

62135-089 is the product NDC for Amoxicillin, Amoxicillin 250 mg/5mL powder, for suspension, listed with the FDA by Chartwell RX, LLC. It has 3 package NDCs, shown above in 10- and 11-digit form.

Chartwell RX, LLC, NDC labeler code 62135. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Amoxicillin NDC 62135-089 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)62135-089Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62135-0089Add 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 NDC	11-digit (billing)	Package
62135-089-01	6213500890162135008901	100 mL in 1 BOTTLE (62135-089-01)Marketed from Jul 16, 2026
62135-089-51	6213500895162135008951	150 mL in 1 BOTTLE (62135-089-51)Marketed from Jul 16, 2026
62135-089-80	6213500898062135008980	80 mL in 1 BOTTLE (62135-089-80)Marketed from Jul 16, 2026

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): Amoxicillin
Generic name (nonproprietary): amoxicillin
Active ingredients: Amoxicillin — 250 mg/5mL
Dosage form: Powder, For suspension
Route: Oral
Labeler: Chartwell RX, LLCNDC labeler code 62135
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 061931
Marketing start: Sep 30, 1990
Listing expires: Dec 31, 2027
Other FDA classes: Penicillins (Chemical structure)
Identifiers: Product ID 62135-089_5d2ff808-124e-a0c7-e063-6294a90a4618SPL ID 5d2ff808-124e-a0c7-e063-6294a90a4618
Pharmacologic class: Penicillin-class Antibacterial

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

N462135008901 followed by a unit qualifier and the quantity

Package 62135-0089-01. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 62135-089

What is NDC 62135-089?: 62135-089 is the product NDC for Amoxicillin, Amoxicillin 250 mg/5mL powder, for suspension, listed with the FDA by Chartwell RX, LLC. It has 3 package NDCs, 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?: Chartwell RX, LLC, NDC labeler code 62135. 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Amoxicillin	Amoxicillin 250 mg/1	CapsuleOral	Northwind Health Company, LLC	82868-088	82868-0088-30
Amoxicillin	Amoxicillin 875 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0734	67046-0734-03
Amoxicillin	Amoxicillin 875 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-4152	68788-4152-02
Amoxicillin	Amoxicillin 500 mg/1	CapsuleOral	Coupler LLC	67046-0316	67046-0316-03
Amoxicillin	Amoxicillin 250 mg/1	CapsuleOral	Coupler LLC	67046-0127	67046-0127-03
Amoxicillin	Amoxicillin 875 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0015	67046-0015-03
Amoxicillin	Amoxicillin 500 mg/1	CapsuleOral	Coupler LLC	67046-1175	67046-1175-03
Amoxicillin	Amoxicillin 875 mg/1	Tablet, CoatedOral	Preferred Pharmaceuticals Inc.	68788-4062	68788-4062-02
Amoxicillin	Amoxicillin 400 mg/5mL	For suspensionOral	REMEDYREPACK INC.	70518-4529	70518-4529-00
Amoxicillin	Amoxicillin 400 mg/5mL	Powder, For suspensionOral	REMEDYREPACK INC.	70518-4522	70518-4522-00

All 275 Amoxicillin NDCs

Other NDCs under ANDA 061931

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

FDA NDC Directory listings under ANDA 061931
Product	Strength	Form · route	Labeler	Product NDC
Amoxicillin	Amoxicillin 250 mg/5mL	Powder, For suspensionOral	Teva Pharmaceuticals USA, Inc.	0093-4155
Amoxicillin	Amoxicillin 125 mg/5mL	Powder, For suspensionOral	Chartwell RX, LLC	62135-109
Amoxicillin	Amoxicillin 250 mg/5mL	Powder, For suspensionOral	Proficient Rx LP	63187-186
Amoxicillin	Amoxicillin 250 mg/5mL	Powder, For suspensionOral	NuCare Pharmaceuticals,Inc.	66267-994
Amoxicillin	Amoxicillin 250 mg/5mL	Powder, For suspensionOral	NuCare Pharmaceuticals,Inc.	68071-2558
Amoxicillin	Amoxicillin 250 mg/5mL	Powder, For suspensionOral	Asclemed USA, Inc.	76420-573