What is NDC 50090-7848?

50090-7848 is the product NDC for Ciprofloxacin Hydrochloride, Ciprofloxacin hydrochloride 500 mg/1 tablet, film coated, listed with the FDA by A-S Medication Solutions. It has 1 package NDC, shown above in 10- and 11-digit form.

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 Hydrochloride?

24 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Ciprofloxacin Hydrochloride NDC 50090-7848

NDC codes

FDA NDC Directory

Product NDC (as listed)50090-7848Labeler and product segments. Claims need a package NDC.

Product NDC at billing width50090-7848Add 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
50090-7848-1	5009078480150090784801	14 TABLET, FILM COATED in 1 BOTTLE (50090-7848-1)Marketed from Jan 5, 2026

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 — 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 076593
Marketing start: May 23, 2024
Listing expires: Dec 31, 2027
Other FDA classes: Cytochrome P450 1A2 Inhibitors (Mechanism)Fluoroquinolones (Chemical structure)
Identifiers: Product ID 50090-7848_0865c2c3-d66b-407c-a9bc-8a25c9f2b20dSPL ID 0865c2c3-d66b-407c-a9bc-8a25c9f2b20dSPL set ID 1057be77-00bb-4839-be3d-c8e11ae531a2RxCUI 309309UNII 4BA73M5E37
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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N450090784801 followed by a unit qualifier and the quantity

Package 50090-7848-01. 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 Jan 8, 2026. This label includes a boxed warning.

Indications (excerpt from the label)

Ciprofloxacin 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 Bronchiti…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 50090-7848

What is NDC 50090-7848?: 50090-7848 is the product NDC for Ciprofloxacin Hydrochloride, Ciprofloxacin hydrochloride 500 mg/1 tablet, film coated, listed with the FDA by A-S Medication Solutions. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: 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 Hydrochloride?: 24 other product NDCs are listed under this name. See all Ciprofloxacin Hydrochloride 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 Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Ciprofloxacin Hydrochloride	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	St. Mary's Medical Park Pharmacy	60760-847	60760-0847-20
Ciprofloxacin Hydrochloride	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-1692	67046-1692-03
Ciprofloxacin Hydrochloride	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc	68788-4177	68788-4177-0068788-4177-0168788-4177-02+2 more
Ciprofloxacin Hydrochloride	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	Advanced Rx of Tennessee, LLC	80425-0493	80425-0493-0180425-0493-02
Ciprofloxacin Hydrochloride	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-7843	50090-7843-0050090-7843-0150090-7843-03+4 more
Ciprofloxacin Hydrochloride	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	Redpharm Drug	67296-2208	67296-2208-02
Ciprofloxacin Hydrochloride	Ciprofloxacin hydrochloride 250 mg/1	Tablet, Film coatedOral	Westminster Pharmaceuticals, LLC	69367-385	69367-0385-01
Ciprofloxacin Hydrochloride	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	Westminster Pharmaceuticals, LLC	69367-386	69367-0386-0169367-0386-05
Ciprofloxacin Hydrochloride	Ciprofloxacin hydrochloride 750 mg/1	Tablet, Film coatedOral	Westminster Pharmaceuticals, LLC	69367-387	69367-0387-50
Ciprofloxacin Hydrochloride	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	72789-577	72789-0577-0672789-0577-1072789-0577-14+2 more

All 25 Ciprofloxacin Hydrochloride NDCs

Other NDCs under ANDA 076593

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

FDA NDC Directory listings under ANDA 076593
Product	Strength	Form · route	Labeler	Product NDC
Ciprofloxacin Hydrochloride	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-7843
Ciprofloxacin Hydrochloride	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	St. Mary's Medical Park Pharmacy	60760-847
Ciprofloxacin Hydrochloride	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-1692
Ciprofloxacin Hydrochloride	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	Redpharm Drug	67296-2208
Ciprofloxacin Hydrochloride	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc	68788-4177
Ciprofloxacin Hydrochloride	Ciprofloxacin hydrochloride 250 mg/1	Tablet, Film coatedOral	Westminster Pharmaceuticals, LLC	69367-385
Ciprofloxacin Hydrochloride	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	Westminster Pharmaceuticals, LLC	69367-386
Ciprofloxacin Hydrochloride	Ciprofloxacin hydrochloride 750 mg/1	Tablet, Film coatedOral	Westminster Pharmaceuticals, LLC	69367-387
Ciprofloxacin Hydrochloride	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	72789-577
Ciprofloxacin Hydrochloride	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	Advanced Rx of Tennessee, LLC	80425-0493
Ciprofloxacin Hydrochloride	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	Proficient Rx LP	82804-260
Ciprofloxacin Hydrochloride	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	VERITYRX, LLC	83939-0002