What is NDC 60505-0582?

60505-0582 is the product NDC for Moxifloxacin, Moxifloxacin hydrochloride monohydrate 5 mg/mL solution/ drops, listed with the FDA by Apotex Corp.. It has 1 package NDC, shown above in 10- and 11-digit form.

What is the active ingredient?

Moxifloxacin hydrochloride monohydrate.

Apotex Corp., NDC labeler code 60505. 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 60505-0582 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)60505-0582Labeler and product segments. Claims need a package NDC.

Product NDC at billing width60505-0582Add 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
60505-0582-4	6050505820460505058204	1 BOTTLE, DROPPER in 1 CARTON (60505-0582-4) / 3 mL in 1 BOTTLE, DROPPERMarketed from Jul 1, 2017

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): Moxifloxacin
Generic name (nonproprietary): moxifloxacin
Active ingredients: Moxifloxacin hydrochloride monohydrate — 5 mg/mL
Dosage form: Solution/ drops
Route: Ophthalmic
Labeler: Apotex Corp.NDC labeler code 60505
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 090080
Marketing start: Jul 1, 2017
Listing expires: Dec 31, 2027
Other FDA classes: Fluoroquinolones (Chemical structure)
Identifiers: Product ID 60505-0582_2ac2915b-7cf9-0e38-d244-9a69134e0954SPL ID 2ac2915b-7cf9-0e38-d244-9a69134e0954
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. Ophthalmic products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N460505058204 followed by a unit qualifier and the quantity

Package 60505-0582-04. 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 60505-0582

What is NDC 60505-0582?: 60505-0582 is the product NDC for Moxifloxacin, Moxifloxacin hydrochloride monohydrate 5 mg/mL solution/ drops, listed with the FDA by Apotex Corp.. 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 monohydrate.
Who is the labeler?: Apotex Corp., NDC labeler code 60505. 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

Other NDCs under ANDA 090080

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

FDA NDC Directory listings under ANDA 090080
Product	Strength	Form · route	Labeler	Product NDC
Moxifloxacin	Moxifloxacin hydrochloride monohydrate 5 mg/mL	Solution/ dropsOphthalmic	Golden State Medical Supply, Inc.	51407-321
Moxifloxacin	Moxifloxacin hydrochloride monohydrate 5 mg/mL	Solution/ dropsOphthalmic	Bryant Ranch Prepack	72162-2107
Moxifloxacin	Moxifloxacin hydrochloride monohydrate 5 mg/mL	Solution/ dropsOphthalmic	Advanced Rx Pharmacy of Tennessee, LLC	80425-0239