Ciprofloxacin Hydrochloride 500 mg Tablet, Film Coated, 20-count
by St. Mary's Medical Park Pharmacy · 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-847-20)
NDC 60760-0847-20
🏷️ FDA NDC (as labeled)
60760-847-20
billing pads the product segment with a zero
Rx only
Generic
On market
Non-controlled
🗂️ Data synced Sep 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
🆔 Identity & classification
FDA NDC (as labeled)
60760-847-20
Product NDC
60760-847
11-digit billing NDC
60760084720
Application #
ANDA076593
SPL Set ID
5bb4a02e-d5ce-7132-e063-6394a90a3010
Established class (EPC)
Fluoroquinolone Antibacterial
Mechanism of action
Cytochrome P450 1A2 Inhibitors
Chemical class
Fluoroquinolones
DEA schedule
Non-controlled
Marketing category
ANDA
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2026-09-17
Route
ORAL
Dosage form
TABLET, FILM COATED
Substance
CIPROFLOXACIN HYDROCHLORIDE
TE code (Orange Book)
AB · RLD · RS
Why two NDCs?
The FDA registers this code as 60760-847-20 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 60760-0847-20. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.
🏭 Manufacturer & labeler
LabelerSt. Mary's Medical Park Pharmacy
Application holderAIPING PHARMACEUTICAL INC
FDA applicationANDA076593 (ANDA)
Labeler code60760
First marketedSep 2026
Product typeHuman Prescription Drug
Portfolio269 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.
🩺 Clinical
📗 Our plain-language guide HelloPharmacist
- Ciprofloxacin treats a wide range of bacterial infections — things like urinary tract infections, skin infections, bone and joint infections, infectious diarrhea, typhoid fever, an...
- What kinds of infections does ciprofloxacin actually treat?
- You can take ciprofloxacin with or without food — that part's flexible. But avoid taking it at the same time as milk, yogurt, or calcium-fortified juices, because dairy and calcium...
- The most common side effects are nausea, diarrhea, and vomiting — uncomfortable, but usually manageable. The ones that mean stop-and-call-your-doctor-now are tendon pain (especiall...
Patient education
Supplement & herbal interactions
11
Nutrient depletion considerations
Ciprofloxacin may be associated with lower levels of 11 nutrients — worth a chat with your pharmacist, not a cause for alarm.
BIOTIN
Insignificant Depletion
CALCIUM
Insignificant Depletion
FOLIC ACID
Insignificant Depletion
IRON
Insignificant Depletion
MAGNESIUM
Insignificant Depletion
+6 more
An association is not a deficiency. Educational only — don't start or stop anything without professional guidance.
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.
💬 Questions about Ciprofloxacin Hydrochloride?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
💊 What it looks like
Color
white
ShapeOval
ImprintE451
Size18 mm
ScoringNot scored
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.
🧪 Inactive Ingredients / Excipients
Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.
💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.
-
UNII 70097M6I30
Magnesium stearate is a salt made from magnesium and stearic acid, a fatty substance. It's used in tablets and capsules as a lubricant and glidant to help ingredients flow smoothly during manufacturing and prevent sticking.
-
UNII 3WJQ0SDW1A
Polyethylene glycol is a synthetic liquid or solid polymer used in medicines as a solvent, lubricant, and humectant. It helps dissolve active ingredients, reduces friction during manufacturing, and retains moisture in the final product.
-
UNII 532B59J990
Polyvinyl alcohol is a synthetic polymer made from plant-derived materials. It's used as a binder to hold ingredients together, a film-former in coatings, and a thickener in liquid formulations.
-
UNII ETJ7Z6XBU4
Silicon dioxide is a naturally occurring mineral used as a glidant and anti-caking agent. It helps powder ingredients flow smoothly and prevents clumping during manufacturing and storage.
-
UNII 5856J3G2A2
A starch-based powder made from potatoes and processed with sodium. It acts as a disintegrant, helping the tablet or capsule break apart quickly in the stomach so the medicine can be absorbed.
-
UNII O8232NY3SJ
A plant-based carbohydrate derived from corn kernels. It acts as a filler to add bulk, a binder to hold ingredients together, and a disintegrant to help the tablet break apart in your stomach for absorption.
-
UNII 7SEV7J4R1U
A powder made from a naturally occurring mineral. In medicines, talc works as a glidant and anti-caking agent, helping tablets and capsules flow smoothly during manufacturing and preventing clumping.
-
UNII 15FIX9V2JP
Titanium dioxide is a bright white mineral powder commonly used as a colorant and opacifying agent. It makes pills and tablets white or lighter in color and helps make coatings non-transparent.
8 inactive ingredients listed in the exact product block matched to this NDC.
Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed —
ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.Inactive ingredient FAQ
Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.
💲 Pricing
A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.
| Price system | Per each | Per package |
|---|---|---|
| Retail pharmacies payNADAC · weekly | Not in the retail survey — common for institutional, discontinued, or low-volume packs. | |
| Medicaid paysCMS SDUD · 12 mo | No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data. | |
| Medicare drug plans payPart D · quarterly | No Part D plan price is available for this NDC in our data. | |
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.
🔁 Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Ciprofloxacin 500 mg 61442-0223-01 | Carlsbad | 100 tablets | $0.123 | AB | Availability likely | — |
| Ciprofloxacin 500 mg 65862-0077-01 | Aurobindo | 100 tablets | $0.123 | AB | Availability likely | — |
| Ciprofloxacin 500 mg 60687-0947-01 | American | 1 tablet | $0.123 | AB | Availability likely | — |
| Ciprofloxacin 500 mg 60687-0860-01 | American | 1 tablet | $0.123 | AB | Availability likely | — |
| Ciprofloxacin Hydrochloride 500 mg 69367-0386-01 | Westminster | 100 tablets | $0.123 | AB | Availability likely | — |
| Ciprofloxacin 500 mg 62135-0309-01 | Chartwell | 100 tablets | $0.123 | AB | Availability likely | — |
| Ciprofloxacin 500 mg 59651-0867-01 | Aurobindo | 100 tablets | $0.123 | AB | Availability likely | — |
| Ciprofloxacin 500 mg 71205-0997-00 | Proficient | 100 tablets | — | AB | FDA listed | — |
| Ciprofloxacin 500 mg 71610-0109-30 | Aphena | 30 tablets | — | AB | FDA listed | — |
| Ciprofloxacin 500 mg 71610-0159-83 | Aphena | 3600 tablets | — | AB | FDA listed | — |
| Ciprofloxacin 500 mg 63629-1010-01 | Bryant | 100 tablets | — | AB | FDA listed | — |
| Ciprofloxacin 500 mg 70934-0965-06 | Denton | 6 tablets | — | AB | Discontinued | — |
| Ciprofloxacin 500 mg 72789-0065-20 | PD-Rx | 20 tablets | — | AB | FDA listed | — |
| Ciprofloxacin 500 mg 00615-8546-10 | NCS | 10 tablets | — | AB | Discontinued | — |
| Ciprofloxacin Hydrochloride 500 mg 83939-0002-01 | VERITYRX, | 1 tablet | — | AB | FDA listed | — |
| Ciprofloxacin Hydrochloride 500 mg 50090-7843-00 | A-S | 20 tablets | — | AB | FDA listed | — |
| Ciprofloxacin 500 mg 72162-1741-02 | Bryant | 14 tablets | — | AB | FDA listed | — |
| Ciprofloxacin Hydrochloride 500 mg 82804-0260-06 | Proficient | 6 tablets | — | AB | FDA listed | — |
| Ciprofloxacin 500 mg 50090-3791-00 | A-S | 20 tablets | — | AB | Discontinued | — |
| Ciprofloxacin 500 mg 51407-0165-01 | Golden | 100 tablets | — | AB | FDA listed | — |
| Cipro 500 mg 50419-0754-01 | Bayer | 100 tablets | — | AB | FDA listed | — |
| Ciprofloxacin 500 mg 51655-0216-20 | Northwind | 20 tablets | — | AB | FDA listed | — |
| Ciprofloxacin 500 mg 72789-0511-10 | PD-Rx | 10 tablets | — | AB | FDA listed | — |
| Ciprofloxacin 500 mg 50090-3852-00 | A-S | 20 tablets | — | AB | Discontinued | — |
| Ciprofloxacin Hydrochloride 500 mg 67296-2208-01 | Redpharm | 10 tablets | — | AB | FDA listed | — |
| Ciprofloxacin Hydrochloride 500 mg 80425-0493-01 | Advanced | 20 tablets | — | AB | FDA listed | — |
| Ciprofloxacin 500 mg 82982-0050-14 | Pharmasource | 14 tablets | — | AB | Discontinued | — |
| Ciprofloxacin 500 mg 43063-0923-02 | PD-Rx | 2 tablets | — | AB | FDA listed | — |
| Ciprofloxacin 500 mg 50090-5373-00 | A-S | 20 tablets | — | AB | Discontinued | — |
| Ciprofloxacin 500 mg 71205-0649-06 | Proficient | 6 tablets | — | AB | FDA listed | — |
| Ciprofloxacin 500 mg 76420-0045-06 | Asclemed | 6 tablets | — | AB | FDA listed | — |
| Ciprofloxacin 500 mg 00615-8630-10 | NCS | 10 tablets | — | AB | FDA listed | — |
| Ciprofloxacin Hydrochloride 500 mg 50090-7848-01 | A-S | 14 tablets | — | AB | FDA listed | — |
| Ciprofloxacin 500 mg 68788-8136-00 | Preferred | 6 tablets | — | AB | FDA listed | — |
| Ciprofloxacin 500 mg 70518-4214-00 | REMEDYREPACK | 30 tablets | — | AB | FDA listed | — |
| Ciprofloxacin 500 mg 72189-0111-14 | DIRECT | 14 tablets | — | AB | FDA listed | — |
| Ciprofloxacin 500 mg 72789-0330-06 | PD-Rx | 6 tablets | — | AB | FDA listed | — |
| Ciprofloxacin 500 mg 59651-0977-15 | Aurobindo | 1500 tablets | — | AB | FDA listed | — |
| Ciprofloxacin 500 mg 71335-1347-00 | Bryant | 7 tablets | — | AB | FDA listed | — |
| Ciprofloxacin 500 mg 71335-2046-00 | Bryant | 7 tablets | — | AB | FDA listed | — |
| Ciprofloxacin 500 mg 72789-0520-06 | PD-Rx | 6 tablets | — | AB | FDA listed | — |
| Ciprofloxacin Hydrochloride 500 mg 72789-0577-14 | PD-Rx | 14 tablets | — | AB | FDA listed | — |
| Ciprofloxacin 500 mg 85534-0047-00 | HAWAII | 6 tablets | — | AB | FDA listed | — |
| Ciprofloxacin Hydrochloride 500 mg 68788-4177-00 | Preferred | 6 tablets | — | AB | FDA listed | — |
| Ciprofloxacin Hydrochloride 500 mg 67046-1692-03 | Coupler | 30 tablets | — | AB | FDA listed | — |
| Ciprofloxacin 500 mg 67296-2291-04 | Redpharm | 14 tablets | — | AB | FDA listed | — |
| Ciprofloxacin Hydrochloride 500 mgthis 60760-0847-20 | St. | 20 tablets | — | AB | FDA listed | — |
About this product: this is a generic version of the medicine. FDA equivalence ratings are shown when available, and other versions are listed above, least expensive first.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.
⏳ Availability & generic status
🏛️
2026
On the market since
Sep 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔓
·
Generic on the market
this product is a generic
✅This is a generic drug
This product is an FDA-approved generic. Other versions of the same drug are listed under Therapeutic equivalents, least expensive first.
Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.
🔬 Reported adverse events (FAERS)
Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Ciprofloxacin Hydrochloride — the ingredient across all brands.
Top reported reactions
Age at onset
Reporter sex
Male · 42%
Female · 58%
Unknown · 0%
Serious outcomes
Reports over time (by year) — tap or hover for the count & year
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 60760-0847-20 You're viewing this | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-847-20) | 2026-09-17 | Active |
🧭 About this NDC listing & data coverage
Finished prescription product
What data is (and isn’t) available for this NDC — tap to expand
| NDC identity (package / product / labeler codes) | ✓ Available |
| Labeler | ✓ Available |
| Product & package description | ✓ Available |
| Marketing category & status | ✓ Available |
| Active ingredient / dosage form / route | ✓ Available |
| FDA label (SPL via DailyMed) | ✓ Available |
| Package photos | ✓ Available |
| Inactive ingredients (structured) | ✓ Available |
| NADAC pharmacy acquisition price (CMS) | — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey. |
| Orange Book / therapeutic-equivalence data | ✓ Available |
| HCPCS J-code billing crosswalk | — Not published for this NDC Most self-administered / retail products have no J-code — that is normal. |
| Medicaid utilization (CMS SDUD) | — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold. |
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.
Questions about this listing
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The FDA registers it as 60760-847-20, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 60760-0847-20, written without dashes as 60760084720. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 60760-0847-20, the first segment (60760) is the labeler code FDA assigned to St. Mary's Medical Park Pharmacy; the middle segment (0847) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (20) identifies this exact package size and type. Together they name one specific package of one specific product.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by St. Mary's Medical Park Pharmacy. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
St. Mary's Medical Park Pharmacy is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as a prescription product, so it is dispensed under a prescriber's order. Your pharmacist can tell you whether any over-the-counter forms of the same medication exist.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.
📄 Full prescribing information FDA SPL
The complete FDA label for this product — the official prescribing information, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
📄 FDA label ▾
No FDA label is on file for this product yet. Labels load from openFDA / DailyMed and refresh weekly.
No label section mentions that — try another word, or open the full label on DailyMed below.
Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA.
Prefer the government’s original formatting? View this label on DailyMed ↗
For educational and professional reference only — not medical advice. Pricing reflects published
NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.