NDC codes

FDA NDC Directory
Product NDC (as listed)50090-3791Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-3791Add the package segment from the table below.

Product information

Brand name (proprietary)
Ciprofloxacin
Generic name (nonproprietary)
ciprofloxacin hydrochloride
Active ingredients
Ciprofloxacin hydrochloride — 500 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
A-S Medication SolutionsNDC labeler code 50090
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 077859
Marketing start
Marketing end
Other FDA classes
Cytochrome P450 1A2 Inhibitors (Mechanism)Fluoroquinolones (Chemical structure)
Identifiers
Product ID 50090-3791_a8ca9c5b-77c7-492c-b145-f6b02260bcf9SPL ID a8ca9c5b-77c7-492c-b145-f6b02260bcf9SPL set ID 9d83b127-ef13-4b2c-aa30-0f54937dc240RxCUI 309309UNII 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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

Product label

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

Indications (excerpt from the label)

Ciprofloxacin tablet is a fluoroquinolone antibacterial indicated in adults (18 years of age and older) with the following infections caused by designated, susceptible bacteria and in pediatric patients where indicated: Skin and Skin Structure Infections ( 1.1 ) Bone and Joint Infections ( 1.2 ) Complicated Intra-Abdominal Infections ( 1.3 ) Infectious Diarrhea ( 1.4 ) Typhoid Fever (Enteric Fever) ( 1.5 ) Uncomplicated Cervical and Urethral Gonorrhea ( 1.6 ) Inhalational Anthrax post-exposure in adult and pediatric patients ( 1.7 ) Plague in adult and pediatric patients ( 1.8 ) Chronic Bacterial Prostatitis ( 1.9 ) Lower Respiratory Tract Infections ( 1.10 ) Acute Exacerbation of Chronic Br…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 50090-3791

What is NDC 50090-3791?
50090-3791 is the product NDC for Ciprofloxacin (ciprofloxacin hydrochloride), Ciprofloxacin hydrochloride 500 mg/1 tablet, film coated, listed with the FDA by A-S Medication Solutions.
What drug is associated with this NDC?
Ciprofloxacin (Ciprofloxacin Hydrochloride).
What is the active ingredient?
Ciprofloxacin hydrochloride.
Who is the labeler?
A-S Medication Solutions, NDC labeler code 50090. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Ciprofloxacin?
168 other product NDCs are listed under this name. See all Ciprofloxacin 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 Ciprofloxacin NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Ciprofloxacinciprofloxacin hydrochlorideCiprofloxacin hydrochloride 500 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-94760687-0947-01
ciprofloxacinCiprofloxacin hydrochloride 250 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC82868-10282868-0102-1482868-0102-20
ciprofloxacinCiprofloxacin hydrochloride 500 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-019355154-0193-00
CiprofloxacinCiprofloxacin hydrochloride 500 mg/1Tablet, Film coatedOralDirect_Rx72189-62772189-0627-1072189-0627-14
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 250 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-887568788-8875-0068788-8875-0168788-8875-02+4 more
CiprofloxacinCiprofloxacin hydrochloride 500 mg/1TabletOralDirect_Rx72189-62372189-0623-1072189-0623-1472189-0623-20
CiprofloxacinCiprofloxacin hydrochloride 250 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-69060760-0690-10
Ciprofloxacinciprofloxacin hydrochlorideCiprofloxacin hydrochloride 500 mg/1Tablet, Film coatedOralNCS HealthCare of KY, LLC dba Vangard Labs0615-863000615-8630-1000615-8630-1400615-8630-20
Ciprofloxacinciprofloxacin hydrochlorideCiprofloxacin hydrochloride 500 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-97759651-0977-0159651-0977-0559651-0977-20+2 more
Ciprofloxacinciprofloxacin hydrochlorideCiprofloxacin hydrochloride 750 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-97859651-0978-0159651-0978-0559651-0978-20+2 more

All 169 Ciprofloxacin NDCs

Other NDCs under ANDA 077859

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

FDA NDC Directory listings under ANDA 077859
ProductStrengthForm · routeLabelerProduct NDC
Ciprofloxacinciprofloxacin hydrochlorideCiprofloxacin hydrochloride 500 mg/1Tablet, Film coatedOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8630
CiprofloxacinCiprofloxacin hydrochloride 500 mg/1Tablet, Film coatedOralQPharma Inc42708-088
Ciprofloxacinciprofloxacin hydrochlorideCiprofloxacin hydrochloride 250 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-2146
Ciprofloxacinciprofloxacin hydrochlorideCiprofloxacin hydrochloride 500 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-3852
Ciprofloxacinciprofloxacin hydrochlorideCiprofloxacin hydrochloride 500 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-5373
Ciprofloxacinciprofloxacin hydrochlorideCiprofloxacin hydrochloride 500 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-216
Ciprofloxacinciprofloxacin hydrochlorideCiprofloxacin hydrochloride 250 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-866
Ciprofloxacinciprofloxacin hydrochlorideCiprofloxacin hydrochloride 500 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-867
Ciprofloxacinciprofloxacin hydrochlorideCiprofloxacin hydrochloride 750 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-873
Ciprofloxacinciprofloxacin hydrochlorideCiprofloxacin hydrochloride 500 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-977
Ciprofloxacinciprofloxacin hydrochlorideCiprofloxacin hydrochloride 750 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-978
Ciprofloxacinciprofloxacin hydrochlorideCiprofloxacin hydrochloride 500 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-860
Ciprofloxacinciprofloxacin hydrochlorideCiprofloxacin hydrochloride 500 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-947
Ciprofloxacinciprofloxacin hydrochlorideCiprofloxacin hydrochloride 250 mg/1Tablet, Film coatedOralAurobindo Pharma Limited65862-076
Ciprofloxacinciprofloxacin hydrochlorideCiprofloxacin hydrochloride 500 mg/1Tablet, Film coatedOralAurobindo Pharma Limited65862-077
Ciprofloxacinciprofloxacin hydrochlorideCiprofloxacin hydrochloride 750 mg/1Tablet, Film coatedOralAurobindo Pharma Limited65862-078
Ciprofloxacinciprofloxacin hydrochlorideCiprofloxacin hydrochloride 500 mg/1Tablet, Film coatedOralRedpharm Drug67296-2291
Ciprofloxacinciprofloxacin hydrochlorideCiprofloxacin hydrochloride 500 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-8136
Ciprofloxacinciprofloxacin hydrochlorideCiprofloxacin hydrochloride 500 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-4214
Ciprofloxacinciprofloxacin hydrochlorideCiprofloxacin hydrochloride 250 mg/1Tablet, Film coatedOralProficient Rx LP71205-636

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