What is NDC 62135-014?

62135-014 is the product NDC for Moxifloxacin, Moxifloxacin hydrochloride 400 mg/1 tablet, film coated, listed with the FDA by Chartwell RX, LLC. It has 1 package NDC, 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 Moxifloxacin?

23 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Moxifloxacin NDC 62135-014 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)62135-014Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62135-0014Add 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	Copy
62135-014-30	6213500143062135001430	30 TABLET, FILM COATED in 1 BOTTLE (62135-014-30)Marketed from Aug 11, 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): Moxifloxacin
Generic name (nonproprietary): moxifloxacin
Active ingredients: Moxifloxacin hydrochloride — 400 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Chartwell RX, LLCNDC labeler code 62135
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 207285
Marketing start: Feb 13, 2017
Listing expires: Dec 31, 2027
Other FDA classes: Fluoroquinolones (Chemical structure)
Identifiers: Product ID 62135-014_59428a91-3a88-2e83-e063-6294a90a3cefSPL ID 59428a91-3a88-2e83-e063-6294a90a3cefSPL set ID 656f582c-ecba-4ec8-9420-9562114d889bRxCUI 311787UNII C53598599TUPC 0362135014308
Pharmacologic class: Fluoroquinolone 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

N462135001430 followed by a unit qualifier and the quantity

Package 62135-0014-30. 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

Current FDA label (SPL), effective Aug 17, 2026. This label includes a boxed warning.

Indications (excerpt from the label)

Moxifloxacin is a fluoroquinolone antibacterial indicated for treating infections in adults 18 years of age and older caused by designated susceptible bacteria, in the conditions listed below: Community Acquired Pneumonia (1.1) Skin and Skin Structure Infections: Uncomplicated (1.2) and Complicated (1.3) Complicated Intra-Abdominal Infections (1.4) Plague (1.5) Acute Bacterial Sinusitis (1.6) Acute Bacterial Exacerbation of Chronic Bronchitis (1.7) To reduce the development of drug-resistant bacteria and maintain the effectiveness of moxifloxacin and other antibacterial drugs. Moxifloxacin should be used only to treat or prevent infections that are proven or strongly suspected to be caused b…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 62135-014

What is NDC 62135-014?: 62135-014 is the product NDC for Moxifloxacin, Moxifloxacin hydrochloride 400 mg/1 tablet, film coated, listed with the FDA by Chartwell RX, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Moxifloxacin.
What is the active ingredient?: Moxifloxacin hydrochloride.
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 Moxifloxacin?: 23 other product NDCs are listed under this name. See all Moxifloxacin 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 Moxifloxacin NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Moxifloxacin	Moxifloxacin hydrochloride 400 mg/1	Tablet, Film coatedOral	Macleods Pharmaceuticals Limited	33342-322	33342-0322-0733342-0322-12
Moxifloxacinmoxifloxacin hydrochloride	Moxifloxacin hydrochloride 400 mg/1	Tablet, Film coatedOral	Solaris Pharma Corporation	73473-903	73473-0903-30
Moxifloxacin	Moxifloxacin hydrochloride monohydrate 5 mg/mL	Solution/ dropsOphthalmic	Advanced Rx Pharmacy of Tennessee, LLC	80425-0379	80425-0379-01
Moxifloxacin	Moxifloxacin hydrochloride 400 mg/1	Tablet, Film coatedOral	Camber Pharmaceuticals, Inc.	31722-845	31722-0845-0531722-0845-30
Moxifloxacin	Moxifloxacin hydrochloride monohydrate 5 mg/mL	Solution/ dropsOphthalmic	Advanced Rx Pharmacy of Tennessee, LLC	80425-0239	80425-0239-01
Moxifloxacin	Moxifloxacin hydrochloride 5 mg/mL	Solution/ dropsOphthalmic	Direct Rx	72189-334	72189-0334-05
Moxifloxacin	Moxifloxacin hydrochloride monohydrate 5 mg/mL	Solution/ dropsOphthalmic	Direct Rx	72189-321	72189-0321-05
Moxifloxacin	Moxifloxacin hydrochloride 5 mg/mL	SolutionOphthalmic	Lupin Pharmaceuticals, Inc.	68180-421	68180-0421-01
Moxifloxacin	Moxifloxacin hydrochloride 5 mg/mL	Solution/ dropsOphthalmic	NorthStar Rx LLC	16714-643	16714-0643-01
Moxifloxacin	Moxifloxacin hydrochloride 5 mg/mL	Solution/ dropsOphthalmic	A-S Medication Solutions	50090-8029	50090-8029-00

All 24 Moxifloxacin NDCs