NDC codes

FDA NDC Directory
Product NDC (as listed)70756-638Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70756-0638Add 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
70756-638-2570756063825707560638251 BOTTLE in 1 CARTON (70756-638-25) / 3 mL in 1 BOTTLEMarketed from Jan 27, 2025

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 ophthalmic solution
Generic name (nonproprietary)
moxifloxacin
Active ingredients
Moxifloxacin hydrochloride — 5 mg/mL
Dosage form
Solution/ drops
Route
Ophthalmic
Labeler
Lifestar Pharma LLCNDC labeler code 70756
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 217988
Marketing start
Listing expires
Other FDA classes
Fluoroquinolones (Chemical structure)
Identifiers
Product ID 70756-638_22d5cd84-26c0-49b0-afbf-1e9155749cf6SPL ID 22d5cd84-26c0-49b0-afbf-1e9155749cf6SPL set ID ca19b837-8e80-408f-af7b-b0464f20c0c3RxCUI 403818UNII C53598599TUPC 0370756638254

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

N470756063825 followed by a unit qualifier and the quantity

Package 70756-0638-25. 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 .

Indications (excerpt from the label)

Moxifloxacin ophthalmic solution is indicated for the treatment of bacterial conjunctivitis caused by susceptible strains of the following organisms: Corynebacterium species* Micrococcus luteus* Staphylococcus aureus Staphylococcus epidermidis Staphylococcus haemolyticus Staphylococcus hominis Staphylococcus warneri* Streptococcus pneumoniae Streptococcus viridans group Acinetobacter lwoffii* Haemophilus influenza Haemophilus parainfluenzae* Chlamydia trachomatis *Efficacy for this organism was studied in fewer than 10 infections. Moxifloxacin ophthalmic solution is a topical fluoroquinolone anti-infective indicated for the treatment of bacterial conjunctivitis caused by susceptible strains …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70756-638

What is NDC 70756-638?
70756-638 is the product NDC for Moxifloxacin ophthalmic solution (moxifloxacin), Moxifloxacin hydrochloride 5 mg/mL solution/ drops, listed with the FDA by Lifestar Pharma LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Moxifloxacin ophthalmic solution (Moxifloxacin).
What is the active ingredient?
Moxifloxacin hydrochloride.
Who is the labeler?
Lifestar Pharma LLC, NDC labeler code 70756. 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 ophthalmic solution?
7 other product NDCs are listed under this name. See all Moxifloxacin ophthalmic solution 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 ophthalmic solution NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Moxifloxacin ophthalmic solutionmoxifloxacinMoxifloxacin hydrochloride 5 mg/mLSolution/ dropsOphthalmicRedpharm Drug67296-222267296-2222-03
Moxifloxacin Ophthalmic Solutionmoxifloxacin ophthalmicMoxifloxacin hydrochloride 5 mg/mLSolution/ dropsOphthalmicFosun Pharma USA Inc.72266-15872266-0158-01
Moxifloxacin Ophthalmic Solutionmoxifloxacin ophthalmicMoxifloxacin hydrochloride 5 mg/mLSolution/ dropsOphthalmicGland Pharma Limited68083-21068083-0210-01
Moxifloxacin ophthalmic solutionMoxifloxacin hydrochloride 5 mg/mLSolution/ dropsOphthalmicAlembic Pharmaceuticals Limited46708-50546708-0505-03
Moxifloxacin ophthalmic solutionmoxifloxacin ophthalmicMoxifloxacin hydrochloride 5 mg/mLSolution/ dropsOphthalmicA-S Medication Solutions50090-478150090-4781-00
Moxifloxacin ophthalmic solutionMoxifloxacin hydrochloride 5 mg/mLSolution/ dropsOphthalmicAlembic Pharmaceuticals Inc.62332-50562332-0505-03
Moxifloxacin Ophthalmic Solutionmoxifloxacin hydrochlorideMoxifloxacin hydrochloride 5 mg/mLSolution/ dropsOphthalmicSandoz Inc0781-713500781-7135-93

Other NDCs under ANDA 217988

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

FDA NDC Directory listings under ANDA 217988
ProductStrengthForm · routeLabelerProduct NDC
Moxifloxacin ophthalmic solutionmoxifloxacinMoxifloxacin hydrochloride 5 mg/mLSolution/ dropsOphthalmicRedpharm Drug67296-2222

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