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⚪no package photo
in the FDA label

moxifloxacin hydrochloride 400 mg Tablet, 500-count

by Torrent Pharmaceuticals Limited · 500 TABLET in 1 BOTTLE (13668-201-05)
NDC 13668-0201-05
🏷️ FDA NDC (as labeled) 13668-201-05 billing pads the product segment with a zero
This package
Contains500-count Pack sizes3 compare ↓
Also comes in: 30 tablets 13668-0201-30 100 tablets 13668-0201-01
Rx only Generic Discontinued Non-controlled ⚠ Discontinued by firm
🗂️ Data synced Mar 13, 2024 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. The listing was last certified through May 2024. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

🆔 Identity & classification

FDA NDC (as labeled) 13668-201-05
Product NDC 13668-201
11-digit billing NDC 13668020105
Application # ANDA200160
Chemical class Quinolone Antimicrobial [EPC], Quinolones
DEA schedule Non-controlled
Marketing category ANDA
Marketing status Discontinued
FDA listing status Discontinued by firm (certified through May 2024)
Route ORAL
Dosage form TABLET
Substance MOXIFLOXACIN HYDROCHLORIDE
Why two NDCs? The FDA registers this code as 13668-201-05 — 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 → 13668-0201-05. 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

LabelerTorrent Pharmaceuticals Limited
Application holderTORRENT PHARMACEUTICALS LTD
FDA applicationANDA200160 (ANDA)
Labeler code13668
Product typeHuman Prescription Drug
Portfolio182 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
  • Yes — you can take moxifloxacin with or without food, and even a big, fatty meal or a cup of yogurt won't affect how well it works. The one thing to watch is timing with antacids,...
  • Can I eat or drink normally while taking moxifloxacin tablets?
  • The most common ones are nausea, diarrhea, headache, and dizziness — these are annoying but usually manageable. What you really need to stop the medication for and call your doctor...
  • What side effects should I actually expect, and which ones should make me stop taking it?
📖 Read our full Moxifloxacin guide →

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
11
Nutrient depletion considerations

Moxifloxacin may be associated with lower levels of 11 nutrients — worth a chat with your pharmacist, not a cause for alarm.

🧪 Full Moxifloxacin nutrient depletion report →
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.

🧪 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.

We could not link this NDC to a current FDA Structured Product Label. An inactive-ingredient list is therefore not available from this source.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

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 systemPer eachPer 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.
Try another pack size: 30 tablets 100 tablets
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

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Moxifloxacin Hydrochloride 400 mg 00904-7407-04 Major 1 tablet $1.343 AB Availability likely —
Moxifloxacin Hydrochloride 400 mg 50268-0576-13 AvPAK 1 tablet $1.343 AB Availability likely —
Moxifloxacin Hydrochloride 400 mg 57237-0156-30 Rising 30 tablets $1.343 AB Availability likely —
Moxifloxacin Hydrochloride 400 mg 65862-0603-30 Aurobindo 30 tablets $1.343 AB Availability likely —
Moxifloxacin Hydrochloride 400 mg 68084-0722-65 American 1 tablet $1.343 AB Availability likely —
Moxifloxacin 400 mg 73473-0903-30 Solaris 30 tablets $1.343 AB Availability likely —
Moxifloxacin Hydrochloride Tablets, 400 mg 72205-0001-05 Novadoz 500 tablets $1.672 AB FDA listed —
Moxifloxacin 400 mg 31722-0845-05 Camber 500 tablets — AB FDA listed —
Moxifloxacin 400 mg 33342-0322-07 Macleods 30 tablets — AB FDA listed —
Moxifloxacin Hydrochloride 400 mg 50090-6609-00 A-S 10 tablets — AB FDA listed —
Moxifloxacin Hydrochloride 400 mg 50090-7244-01 A-S 7 tablets — AB FDA listed —
Moxifloxacin Hydrochloride 400 mg 50090-7665-00 A-S 30 tablets — AB FDA listed —
Moxifloxacin 400 mg 55111-0112-01 Dr. 100 tablets — AB FDA listed —
Moxifloxacin 400 mg 63629-8357-01 Bryant 7 tablets — AB FDA listed —
Moxifloxacin Hydrochloride 400 mg 70518-3738-00 REMEDYREPACK 7 tablets — AB FDA listed —
Moxifloxacin Hydrochloride Tablets, 400 mg 70518-4312-00 REMEDYREPACK 7 tablets — AB FDA listed —
Moxifloxacin Hydrochloride 400 mg 70518-4458-00 REMEDYREPACK 7 tablets — AB FDA listed —
Moxifloxacin Hydrochloride 400 mg 71335-2329-01 Bryant 7 tablets — AB FDA listed —
Moxifloxacin Hydrochloride 400 mg 71335-2815-01 Bryant 7 tablets — AB FDA listed —
Moxifloxacin Hydrochloride 400 mg 72789-0037-10 PD-Rx 10 tablets — AB FDA listed —
Moxifloxacin Hydrochloride 400 mg 72789-0038-10 PD-Rx 10 tablets — AB FDA listed —
Moxifloxacin Hydrochloride Tablets, 400 mg 72789-0080-10 PD-Rx 10 tablets — AB FDA listed —
Moxifloxacin 400 mg 72789-0233-10 PD-Rx 10 tablets — AB FDA listed —
Moxifloxacin Hydrochloride 400 mg 72789-0350-10 PD-Rx 10 tablets — AB FDA listed —
moxifloxacin hydrochloride 400 mgthis 13668-0201-05 Torrent 500 tablets — — Discontinued —
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
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.

📦 Packaging — all sizes for this product

Package NDCDescription Per unit Per pack Marketing startStatus
13668-0201-01 100 TABLET in 1 BOTTLE (13668-201-01) — — 2014-04-03 Discontinued by firm
13668-0201-05 You're viewing this 500 TABLET in 1 BOTTLE (13668-201-05) — — 2014-04-03 Discontinued by firm
13668-0201-30 30 TABLET in 1 BOTTLE (13668-201-30) $1.67 / ea $50.16 2014-04-03 Discontinued by firm

You're viewing the largest of 3 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 13668-0201-05?
NDC 13668-0201-05 is a 500-count package — 500 tablet in 1 bottle.
What is the difference between NDC 13668-0201-05 and NDC 13668-0201-30?
Both are moxifloxacin hydrochloride 400 mg Tablet — the drug itself is identical. NDC 13668-0201-05 is the 500-count package, while NDC 13668-0201-30 is the 30 tablets package.
What NDC number is used to bill for this package of moxifloxacin hydrochloride 400 mg Tablet?
Bill NDC 13668-0201-05 — the 11-digit billing format is 13668020105. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Prices are the latest CMS NADAC pharmacy acquisition cost per NDC; per-pack figures are per-unit × pack quantity, shown only when the pack is denominated in the same measure NADAC prices.

🧭 About this NDC listing & data coverage

Finished prescription product No longer marketed (per FDA listing data)
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) — Not published for this NDC No structured label is linked to this listing in DailyMed/openFDA.
Package photos — Not published for this NDC The FDA label for this product carries no photos.
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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 — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
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.
Why is there no full label on this page?
No structured FDA label (SPL) is currently linked to this NDC in DailyMed/openFDA. That can happen with older listings, certain OTC and repackaged products, and recently updated listings whose label has not yet propagated. The listing itself is still valid — this page shows everything the public feeds provide for this package.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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 13668-201-05, 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: 13668-0201-05, written without dashes as 13668020105. 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 13668-0201-05, the first segment (13668) is the labeler code FDA assigned to Torrent Pharmaceuticals Limited; the middle segment (0201) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (05) identifies this exact package size and type. Together they name one specific package of one specific product.
Does this product come in other package sizes?
Yes — the FDA directory lists 2 other package presentations of this same product, including 30 tablets (13668-0201-30), 100 tablets (13668-0201-01). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
Torrent Pharmaceuticals Limited 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
📄 FDA label 19 words ▾

No FDA label is on file for this product yet. Labels load from openFDA / DailyMed and refresh weekly.

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA.
← 13668-0190-05 · Torrent 13668-0202-05 · Torrent →
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.