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, 100-count — NDC 70771-1938-1 (Billing 70771-1938-01)
by Zydus Lifesciences Limited · 100 TABLET in 1 BOTTLE
This is a package of 100 tablets of Trazodone Hydrochloride 50 mg Tablet from Zydus Lifesciences Limited, marketed since Jan 2026 and currently FDA-listed.
NDC 70771-1938-01
🏷️ FDA NDC (as labeled)
70771-1938-1
billing pads the package segment with a zero
This package
Contains100-count
Pack sizes3 compare ↓
Also priced by: Part D plans $0.2383/unit — full pricing hub ↓
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
⚠️
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)
70771-1938-1
Product NDC
70771-1938
11-digit billing NDC
70771193801
UNII
6E8ZO8LRNM
UPC
0368382808011, 0368382609014
Application #
ANDA205253
SPL Set ID
43d4be17-5fae-4326-a5c4-9e25e2db6a43
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
2026-01-22
Route
ORAL
Dosage form
TABLET
Substance
TRAZODONE HYDROCHLORIDE
TE code (Orange Book)
AB · RLD · RS
Quick answers
- RxCUI (RxNorm): 856364
Why two NDCs?
The FDA registers this code as 70771-1938-1 — a 5-4-1 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 package segment → 70771-1938-01. 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.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 1, 2026
RxNorm drug class
This medicine belongs to the Serotonin Reuptake Inhibitor class.
Pharmacologic class
Serotonin Reuptake Inhibitor
Drug family (ATC)
Other antidepressants
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.
- RxClass (NLM) · catalog refreshed Oct 1, 2026
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...
Patient education
Supplement & herbal interactions
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.
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.
- MedlinePlus (NLM) · refreshed Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
💬 Questions about Trazodone Hydrochloride?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
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 · Q2 2026 | $0.2383 | $23.83 / 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.
- CMS NADAC weekly file
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · refreshed Oct 2, 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 70771-1938-00 70771-1938-0 Main listing | 1000 TABLET in 1 BOTTLE | 2026-01-22 | — | Active |
| 70771-1938-01 You're viewing this | 100 TABLET in 1 BOTTLE | 2026-01-22 | — | Active |
| 70771-1938-05 70771-1938-5 | 500 TABLET in 1 BOTTLE | 2026-01-22 | — | Active |
You're viewing the smallest of 3 pack sizes for this product.
Pack size FAQ
What quantity is in this package?
This is a 100-count package — 100 tablet in 1 bottle.
How does this package differ from NDC 70771-1938-05?
Both are Trazodone Hydrochloride 50 mg Tablet — the drug itself is identical. This page's package is the 100-count one, while NDC 70771-1938-05 is the 500 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
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Trazodone Hydrochloride 50 mg 00904-6868-61 | Major | 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 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 60687-0443-01 | American | 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 68382-0609-01 | Zydus | 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 70010-0231-01 | Granules | 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 00615-8371-05 | NCS | 15 tablets | — | AB | Discontinued | — |
| Trazodone Hydrochloride 50 mg 42291-0868-10 | AvKARE | 1000 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 50 mg 45865-0167-30 | Medsource | 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 50090-7943-00 | A-S | 30 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 50 mg 50090-7944-00 | A-S | 90 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 50 mg 51407-0946-01 | Golden | 100 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 50 mg 51655-0366-26 | Northwind | 90 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 50 mg 55154-8087-00 | Cardinal | 10 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 50 mg 60505-2653-00 | Apotex | 100 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 50 mg 67046-1506-03 | Coupler | 30 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 68788-7118-01 | Preferred | 100 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 50 mg 69584-0884-10 | Oxford | 100 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 50 mg 70518-2929-00 | REMEDYREPACK | 30 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 50 mg 70518-3290-01 | REMEDYREPACK | 30 tablets | — | AB | Discontinued | — |
| Trazodone Hydrochloride 50 mg 70518-4363-00 | REMEDYREPACK | 60 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 50 mg 70518-4441-00 | REMEDYREPACK | 30 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 50 mg 70771-1128-00 | Zydus | 1000 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 50 mgthis 70771-1938-01 | Zydus | 100 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 50 mg 71205-0505-30 | Proficient | 30 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 50 mg 71205-0551-30 | Proficient | 30 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 50 mg 71205-0568-30 | Proficient | 30 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 50 mg 71335-0705-00 | Bryant | 14 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 50 mg 71335-1575-00 | Bryant | 14 tablets | — | AB | Discontinued | — |
| Trazodone Hydrochloride 50 mg 71335-2651-00 | Bryant | 14 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 50 mg 71610-0514-30 | Aphena | 30 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 50 mg 71610-0525-15 | Aphena | 15 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 72789-0154-30 | PD-Rx | 30 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 50 mg 76420-0672-01 | Asclemed | 100 tablets | — | AB | FDA listed | — |
| Trazodone Hcl 50 mg 80425-0176-01 | Advanced | 30 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 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 | — |
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.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA Orange Book · refreshed Sep 3, 2026
- CMS NADAC weekly file
Availability & generic status
🏛️
2026
On the market since
Jan 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.
- FDA Orange Book · refreshed Sep 3, 2026
What it looks like
Color
White
ShapeRound
Imprint06
Size1 mm
ScoringScored — splits in 2
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.
- FDA label on DailyMed · label index refreshed Oct 1, 2026
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.
Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
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.- FDA label on DailyMed · label index refreshed Oct 1, 2026
- FDA openFDA NDC Directory · synced Oct 1, 2026
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
LabelerZydus Lifesciences Limited
Application holderZYDUS PHARMACEUTICALS USA INC
FDA applicationANDA205253 (ANDA)
Labeler code70771
First marketedJan 2026
Product typeHuman Prescription Drug
Portfolio720 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.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- Drugs@FDA
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.
💬 Medication Guide ▾
SPL MEDGUIDE
📄 Package Label / Principal Display Panel ▾
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL NDC 70771-1128-1 Trazodone Hydrochloride Tablets USP, 50 mg 100 Tablets Rx only NDC 70771-1129-1 Trazodone Hydrochloride Tablets USP, 100 mg 100 Tablets Rx only NDC 70771-1130-1 Trazodone Hydrochloride Tablets USP, 150 mg 100 Tablets Rx only NDC 70771-1131-1 Trazodone Hydrochloride Tablets USP, 300 mg 100 Tablets Rx only NDC 70771-1938-1 Trazodone Hydrochloride Tablets USP, 50 mg 100 Tablets Rx only NDC 70771-1939-1 Trazodone Hydrochloride Tablets USP, 100 mg 100 Tablets Rx only Trazodone Hyadrochloride Tablets, USP Trazodone Hyadrochloride Tablets, USP Trazodone Hyadrochloride Tablets, USP Trazodone Hyadrochloride Tablets, USP image image
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 ↗
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) | — 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 | ✓ 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 Zydus Lifesciences Limited. 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 2 other package presentations of this same product, including 500 tablets (70771-1938-05), 1000 tablets (70771-1938-00). 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?
Zydus Lifesciences 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.
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.