NDC codes

FDA NDC Directory
Product NDC (as listed)68071-3351Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68071-3351Add 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
68071-3351-36807133510310 mL in 1 BOX (68071-3351-3)Marketed from Jul 20, 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)
Ciprofloxacin Hydrochloride
Generic name (nonproprietary)
ciprofloxacin hydrochloride
Active ingredients
Ciprofloxacin hydrochloride — 3 mg/mL
Dosage form
Solution/ drops
Route
Ophthalmic
Product type
Prescription drug
Marketing category
NDA authorized genericApplication NDA 019992
Marketing start
Listing expires
Other FDA classes
Cytochrome P450 1A2 Inhibitors (Mechanism)Fluoroquinolones (Chemical structure)
Identifiers
Product ID 68071-3351_1ce8f03a-6915-908c-e063-6394a90a270cSPL ID 1ce8f03a-6915-908c-e063-6394a90a270cSPL set ID 54c73290-bd89-3453-e054-00144ff88e88RxCUI 309307UNII 4BA73M5E37

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

N468071335103 followed by a unit qualifier and the quantity

Package 68071-3351-03. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under NDA 019992

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

FDA NDC Directory listings under NDA 019992
ProductStrengthForm · routeLabelerProduct NDC
Ciprofloxacin HydrochlorideCiprofloxacin hydrochloride 3 mg/mLSolution/ dropsOphthalmicNuCare Pharmaceuticals,Inc.68071-4235
Ciprofloxacin HydrochlorideCiprofloxacin hydrochloride 3 mg/mLSolution/ dropsOphthalmicAsclemed USA, Inc.76420-942
Ciprofloxacin HydrochlorideCiprofloxacin hydrochloride 3 mg/mLSolution/ dropsOphthalmicProficient Rx LP63187-985
Ciprofloxacin HydrochlorideCiprofloxacin hydrochloride 3 mg/mLSolution/ dropsOphthalmicA-S Medication Solutions50090-1754
Ciprofloxacin HydrochlorideCiprofloxacin hydrochloride 3 mg/mLSolution/ dropsOphthalmicPreferred Pharmaceuticals Inc.68788-8198
Ciprofloxacin HydrochlorideCiprofloxacin hydrochloride 3 mg/mLSolution/ dropsOphthalmicA-S Medication Solutions50090-0882
Ciprofloxacin HydrochlorideCiprofloxacin hydrochloride 3 mg/mLSolution/ dropsOphthalmicSandoz Inc61314-656
Ciprofloxacin HydrochlorideCiprofloxacin hydrochloride 3 mg/mLSolution/ dropsOphthalmicREMEDYREPACK INC.70518-1170
Ciprofloxacin HydrochlorideCiprofloxacin hydrochloride 3 mg/mLSolution/ dropsOphthalmicRedpharm Drug67296-0142
Ciprofloxacin HydrochlorideCiprofloxacin hydrochloride 3 mg/mLSolution/ dropsOphthalmicNuCare Pharmaceuticals,Inc.68071-4139

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