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Trazodone Hydrochloride 50 mg Tablet, 500-count — NDC 87063-0320-05 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Trazodone Hydrochloride 50 mg Tablet, 500-count — NDC 87063-320-05 (Billing 87063-0320-05)

by ASCLEMED USA INC. · 500 TABLET in 1 BOTTLE

This is a package of 500 tablets of Trazodone Hydrochloride 50 mg Tablet from ASCLEMED USA INC., marketed since Nov 2013 and currently FDA-listed.

NDC 87063-0320-05
🏷️ FDA NDC (as labeled) 87063-320-05 billing pads the product segment with a zero
This package
Contains500-count Pack sizes5 compare ↓
Product page 87063-0320-01 Also comes in: 30 tablets 87063-320-30 60 tablets 87063-320-60 90 tablets 87063-320-90 100 tablets 87063-320-01
Rx only Generic On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Oct 8, 2026 · 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

NDC database record

One package, one record: these facts belong to NDC 87063-320-05 alone.

Record
FDA NDC Directory package listing · Human prescription drug
Code segments
87063 labeler · 320 product · 05 package
Package marketed since
Sep 25, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 8706332005 5
FDA record last changed
Oct 8, 2026
⚠️
Other active recalls for Trazodone Hydrochloride (different manufacturers) — 3 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Aug 24, 2026 — Presence of Foreign Tablets/Capsules (Teva Pharmaceuticals USA, Inc) · FDA recall D-0834-2026
Class II · Jan 26, 2026 — Presence of Foreign Tablets/Capsules (Granules Pharmaceuticals Inc.) · FDA recall D-0305-2026
Class III · Dec 19, 2025 — Failed Tablet/Capsule Specifications: Product complaint received that some tablets had a dent on the plain side of the tablet surface. (Zydus Pharmaceuticals (USA) Inc) · FDA recall D-0247-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 87063-320-05
Product NDC 87063-320
11-digit billing NDC 87063032005
Application # ANDA202180
SPL Set ID 5c52ea35-c2be-b462-e063-6294a90a19c1
Established class (EPC) Serotonin Reuptake Inhibitor
DEA schedule Non-controlled
Marketing category ANDA
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2013-11-27
Route ORAL
Dosage form TABLET
Substance TRAZODONE HYDROCHLORIDE
TE code (Orange Book) AB · RLD · RS
Why two NDCs? The FDA registers this code as 87063-320-05 — 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 → 87063-0320-05. 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.

Clinical

📗 Our plain-language guide HelloPharmacist
  • It treats major depressive disorder in adults. It comes as tablets and as Raldesy oral solution. Your prescriber will decide if it's right for you.
  • Take it by mouth shortly after a meal or light snack, in divided doses as directed. If it makes you drowsy, your prescriber may have you take most of the dose at bedtime. Follow th...
  • Please don't stop suddenly. The dose should be lowered gradually, and your prescriber will guide you.
  • Drowsiness, dizziness, dry mouth, blurred vision, fatigue, headache and nausea are common. Stand up slowly, and use caution driving until you know how it affects you. Call your doc...
📖 Read our full Trazodone guide →

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
1
Nutrient depletion considerations

Trazodone may be associated with lower levels of 1 nutrient — worth a chat with your pharmacist, not a cause for alarm.

🧪 Full Trazodone 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.

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 60 tablets 90 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
87063-0320-01 87063-320-01 Main listing 100 TABLET in 1 BOTTLE 2026-09-25 — Active
87063-0320-05 You're viewing this 500 TABLET in 1 BOTTLE 2026-09-25 — Active
87063-0320-30 87063-320-30 30 TABLET in 1 BOTTLE 2026-09-25 — Active
87063-0320-60 87063-320-60 60 TABLET in 1 BOTTLE 2026-09-25 — Active
87063-0320-90 87063-320-90 90 TABLET in 1 BOTTLE 2026-09-25 — Active

You're viewing the largest of 5 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This is a 500-count package — 500 tablet in 1 bottle.
How does this package differ from NDC 87063-0320-30?
Both are Trazodone Hydrochloride 50 mg Tablet — the drug itself is identical. This page's package is the 500-count one, while NDC 87063-0320-30 is the 30 tablets package.
What NDC number is used to bill for this package of Trazodone Hydrochloride 50 mg Tablet?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Trazodone Hydrochloride 50 mg 68382-0609-01 Zydus 100 tablets $0.031 AB Availability likely —
Trazodone Hydrochloride 50 mg 13107-0079-01 Aurolife 100 tablets $0.031 AB Availability likely —
Trazodone Hydrochloride 50 mg 13668-0330-01 Torrent 100 tablets $0.031 AB Availability likely —
Trazodone Hydrochloride 50 mg 68382-0805-01 Zydus 100 tablets $0.031 AB Availability likely —
Trazodone Hydrochloride 50 mg 00904-6868-61 Major 100 tablets $0.031 AB Availability likely —
Trazodone Hydrochloride 50 mg 70010-0231-01 Granules 100 tablets $0.031 AB Availability likely —
Trazodone Hydrochloride 50 mg 60687-0443-01 American 100 tablets $0.031 AB Availability likely —
Trazodone Hydrochloride 50 mg 50111-0560-01 Teva 100 tablets $0.031 AB Availability likely —
Trazodone Hydrochloride 50 mg 57664-0014-72 Sun 100 tablets $0.031 AB Availability likely —
Trazodone Hydrochloride 50 mg 64980-0672-01 Rising 100 tablets $0.031 AB Availability likely —
Trazodone Hydrochloride 50 mg 60687-0954-01 American 100 tablets $0.031 AB Availability likely —
Trazodone Hydrochloride 50 mg 16729-0299-01 Accord 100 tablets $0.033 AB Availability likely —
Trazodone Hydrochloride 50 mg 71205-0505-30 Proficient 30 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 71205-0568-30 Proficient 30 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 71610-0514-30 Aphena 30 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 50090-5218-00 A-S 30 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 50090-6603-00 A-S 90 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 69584-0884-10 Oxford 100 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 80425-0326-01 Advanced 30 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 80425-0502-01 Advanced 30 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 76420-0672-01 Asclemed 100 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 00615-8371-05 NCS 15 tablets — AB Discontinued —
Trazodone Hydrochloride 50 mg 60505-2653-00 Apotex 100 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 70771-1128-00 Zydus 1000 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 50090-7943-00 A-S 30 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 70518-3290-01 REMEDYREPACK 30 tablets — AB Discontinued —
Trazodone Hydrochloride 50 mg 71335-0705-00 Bryant 14 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 70771-1938-00 Zydus 1000 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 45865-0167-30 Medsource 30 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 51655-0366-26 Northwind 90 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 67046-1506-03 Coupler 30 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 68788-7118-01 Preferred 100 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 71335-2651-00 Bryant 14 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 72789-0154-30 PD-Rx 30 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 50090-7944-00 A-S 90 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 71205-0551-30 Proficient 30 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 71610-0525-15 Aphena 15 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 42291-0868-10 AvKARE 1000 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 51407-0946-01 Golden 100 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 68071-2996-09 NuCare 90 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 68071-4410-02 NuCare 20 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 70518-2929-00 REMEDYREPACK 30 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 70518-4363-00 REMEDYREPACK 60 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 71335-1575-00 Bryant 14 tablets — AB Discontinued —
Trazodone Hydrochloride 50 mg 55154-8087-00 Cardinal 10 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 70518-4441-00 REMEDYREPACK 30 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 71610-0529-30 Aphena 30 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 71610-0874-30 Aphena 30 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 67046-1684-03 Coupler 30 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 87441-0081-01 Unit 30 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 72789-0591-90 PD-Rx 90 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mg 70518-4760-00 REMEDYREPACK 100 tablets — AB FDA listed —
Trazodone Hydrochloride 50 mgthis 87063-0320-05 ASCLEMED 500 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

🏛️
2013
On the market since
Nov 2013
📍
2026
Currently FDA-listed
13 years listed
🔓
·
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.

What it looks like

Color white
ShapeOval
Imprint13;32;505050
Size17 mm
ScoringScore: 3
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.

🧪 Avoiding an ingredient? See Trazodone inactive ingredients by manufacturer: every current product's list side by side, so you can ask your pharmacy for the version that does not list it.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII OP1R32D61U
    Microcrystalline cellulose is a purified form of cellulose, a natural fiber from plant sources. It acts as a binder and filler in tablets and capsules, helping hold ingredients together and give the medicine its shape and size.
  • 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 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 368GB5141J
    A detergent and foaming agent derived from coconut or palm oil. In medications, it helps break down and mix oil and water-based ingredients, aids in tablet disintegration, and improves how the drug dissolves and spreads in the mouth or digestive system.
  • 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.

6 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.

Manufacturer & labeler

LabelerASCLEMED USA INC.
Application holderTORRENT PHARMACEUTICALS LTD
FDA applicationANDA202180 (ANDA)
Labeler code87063
First marketedNov 2013
Product typeHuman Prescription Drug
Portfolio136 products on file

More NDCs from ASCLEMED USA INC. labeler code 87063

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.

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. Prefer the government’s original formatting? View this label on DailyMed ↗

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 form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
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 ASCLEMED USA INC.. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 4 other package presentations of this same product, including 30 tablets (87063-0320-30), 60 tablets (87063-0320-60), 90 tablets (87063-0320-90). 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?
ASCLEMED USA INC. 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.
← 87063-0309-01 · ASCLEMED 87063-0321-01 · ASCLEMED →
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.