NDC codes

FDA NDC Directory
Product NDC (as listed)76420-273Labeler and product segments. Claims need a package NDC.
Product NDC at billing width76420-0273Add 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
76420-273-10764200273107642002731010 mL in 1 BOTTLE (76420-273-10)Marketed from Sep 7, 2022

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)
Cipro HcSuffix: HC
Generic name (nonproprietary)
ciprofloxacin hydrochloride and hydrocortisone
Active ingredients
Ciprofloxacin hydrochloride — 2 mg/mLHydrocortisone — 10 mg/mL
Dosage form
Suspension/ drops
Route
Auricular (Otic)
Labeler
Asclemed USA, Inc.NDC labeler code 76420
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 020805
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)Quinolones (Chemical structure)
Identifiers
Product ID 76420-273_e80fc4b5-cf91-6430-e053-2995a90a8128SPL ID e80fc4b5-cf91-6430-e053-2995a90a8128SPL set ID eafad445-2735-434b-a1c6-e1c6b201d2cfRxCUI 213320, 309305UNII 4BA73M5E37, WI4X0X7BPJ
Pharmacologic class
Corticosteroid; Quinolone Antimicrobial

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N476420027310 followed by a unit qualifier and the quantity

Package 76420-0273-10. 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)

INDICATIONS AND USAGE CIPRO ® HC OTIC is indicated for the treatment of acute otitis externa in adult and pediatric patients, one year and older, due to susceptible strains of Pseudomonas aeruginosa , Staphylococcus aureus , and Proteus mirabilis .

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 76420-273

What is NDC 76420-273?
76420-273 is the product NDC for Cipro Hc, Ciprofloxacin hydrochloride 2 mg/mL; Hydrocortisone 10 mg/mL suspension/ drops, listed with the FDA by Asclemed USA, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Cipro Hc (Ciprofloxacin hydrochloride and hydrocortisone).
What is the active ingredient?
Ciprofloxacin hydrochloride, Hydrocortisone.
Who is the labeler?
Asclemed USA, Inc., NDC labeler code 76420. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Cipro Hc?
3 other product NDCs are listed under this name. See all Cipro Hc 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 Cipro Hc NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Cipro Hcciprofloxacin hydrochloride and hydrocortisoneCiprofloxacin hydrochloride 2 mg/mL; Hydrocortisone 10 mg/mLSuspension/ dropsAuricular (Otic)A-S Medication Solutions50090-604350090-6043-00
Cipro Hcciprofloxacin hydrochloride and hydrocortisoneCiprofloxacin hydrochloride 2 mg/mL; Hydrocortisone 10 mg/mLSuspension/ dropsAuricular (Otic)A-S Medication Solutions50090-763150090-7631-00
Cipro Hcciprofloxacin hydrochloride and hydrocortisoneCiprofloxacin hydrochloride 2 mg/mL; Hydrocortisone 10 mg/mLSuspension/ dropsAuricular (Otic)Sandoz Inc66758-08766758-0087-70

Other NDCs under NDA 020805

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

FDA NDC Directory listings under NDA 020805
ProductStrengthForm · routeLabelerProduct NDC
Cipro Hcciprofloxacin hydrochloride and hydrocortisoneCiprofloxacin hydrochloride 2 mg/mL; Hydrocortisone 10 mg/mLSuspension/ dropsAuricular (Otic)A-S Medication Solutions50090-6043
Cipro Hcciprofloxacin hydrochloride and hydrocortisoneCiprofloxacin hydrochloride 2 mg/mL; Hydrocortisone 10 mg/mLSuspension/ dropsAuricular (Otic)A-S Medication Solutions50090-7631
Cipro Hcciprofloxacin hydrochloride and hydrocortisoneCiprofloxacin hydrochloride 2 mg/mL; Hydrocortisone 10 mg/mLSuspension/ dropsAuricular (Otic)Sandoz Inc66758-087
ciprofloxacin hydrochloride and hydrocortisoneCiprofloxacin hydrochloride 2 mg/mL; Hydrocortisone 10 mg/mLSuspension/ dropsAuricular (Otic)Sandoz Inc0781-6218

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