Trazodone Hydrochloride 100 mg Tablet, 30-count — NDC 72789-168-30 (Billing 72789-0168-30)
by PD-Rx Pharmaceuticals, Inc. · 30 TABLET in 1 BOTTLE, PLASTIC
This is a package of 30 tablets of Trazodone Hydrochloride 100 mg Tablet from PD-Rx Pharmaceuticals, Inc., marketed since Dec 2017 and currently FDA-listed, this package's marketing is listed to end Feb 2027. It is the main listing for this product, which comes in 2 package sizes.
NDC 72789-0168-30
🏷️ FDA NDC (as labeled)
72789-168-30
billing pads the product segment with a zero
This package
Contains30-count
Pack sizes2 compare ↓
Main listing for product 72789-168 · Also comes in:
90 tablets 72789-168-90
🗂️ FDA directory synced Oct 8, 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 →
NDC database record
One package, one record: these facts belong to NDC 72789-168-30 alone.
- Record
- FDA NDC Directory package listing · Human prescription drug
- Code segments
- 72789 labeler · 168 product · 30 package
- Package marketed since
- Mar 25, 2021
- Package marketing ended
- Feb 28, 2027
- Sample package
- No — commercial package
- Billing quantity
- 30 EA per package
- Barcode (UPC-A, from the NDC)
- 3 7278916830 2
- 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)
72789-168-30
Product NDC
72789-168
11-digit billing NDC
72789016830
NCPDP billing unit
EA — each (per item)
Application #
ANDA205253
SPL Set ID
5b366b0a-80e3-3515-e063-6294a90a5035
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
2017-12-11
Marketing end
2027-02-28
Route
ORAL
Dosage form
TABLET
Substance
TRAZODONE HYDROCHLORIDE
TE code (Orange Book)
AB · RLD · RS
Drug-database identifiers Medi-Span GPI and First Databank GCN / HICL / AHFS classification
GCN Seq No
046242
GCN
16392
HICL code
001652
Ingredient (HICL)
Trazodone Hcl
HIC1 code
H
Therapeutic class — broad (HIC1)
Nervous System (Except Autonomic)
HIC2 code
H7
Therapeutic class — intermediate (HIC2)
Psychoactive Drugs (Continued 1)
HIC3 code
H7E
Therapeutic class — specific (HIC3)
Serotonin-2 Antagonist/Reuptake Inhibitors (Saris)
AHFS code
28:16.04.24
AHFS class
Serotonin Modulators
FDB label name
TRAZODONE 100 MG TABLET
FDB brand name
Trazodone Hcl
Legend status
F — Federal legend — prescription drug or device
Quick answers
- GSN (GCN sequence number): 046242
- GCN: 16392
- HICL (First Databank): 001652
- AHFS class code: 28:16.04.24
Why two NDCs?
The FDA registers this code as 72789-168-30 — 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 → 72789-0168-30. 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 8, 2026
- FDA label on DailyMed · label index refreshed Oct 6, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 8, 2026
Clinical
Label name TRAZODONE 100 MG TABLET Ingredient Trazodone Hcl
📖 What it is MedlinePlus · NLM
Trazodone is used to treat depression. Trazodone is in a class of medications called serotonin modulators. It works by increasing the amount of serotonin, a natural substance in the brain that helps maintain mental balance.
Read the full MedlinePlus article ↗📗 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 6, 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 · 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:
90 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 8, 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 |
|---|---|---|---|---|
| 72789-0168-30 You're viewing this Main listing | 30 TABLET in 1 BOTTLE, PLASTIC | 2021-03-25 | Feb 28, 2027 | Active |
| 72789-0168-90 72789-168-90 | 90 TABLET in 1 BOTTLE, PLASTIC | 2021-02-22 | Feb 28, 2027 | Active |
You're viewing the smallest of 2 pack sizes for this product.
Pack size FAQ
What quantity is in this package?
This is a 30-count package — 30 tablet in 1 bottle, plastic.
How does this package differ from NDC 72789-0168-90?
Both are Trazodone Hydrochloride 100 mg Tablet — the drug itself is identical. This page's package is the 30-count one, while NDC 72789-0168-90 is the 90 tablets package.
What NDC number is used to bill for this package of Trazodone Hydrochloride 100 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 100 mg 16729-0300-01 | Accord | 100 tablets | $0.050 | AB | Availability likely | — |
| Trazodone Hydrochloride 100 mg 00904-6869-61 | Major | 100 tablets | $0.051 | AB | Availability likely | — |
| Trazodone Hydrochloride 100 mg 13107-0080-01 | Aurolife | 100 tablets | $0.051 | AB | Availability likely | — |
| Trazodone Hydrochloride 100 mg 13668-0331-01 | Torrent | 100 tablets | $0.051 | AB | Availability likely | — |
| Trazodone Hydrochloride 100 mg 50111-0561-01 | Teva | 100 tablets | $0.051 | AB | Availability likely | — |
| Trazodone Hydrochloride 100 mg 57664-0026-72 | Sun | 100 tablets | $0.051 | AB | Availability likely | — |
| Trazodone Hydrochloride 100 mg 60687-0454-01 | American | 100 tablets | $0.051 | AB | Availability likely | — |
| Trazodone Hydrochloride 100 mg 64980-0673-01 | Rising | 100 tablets | $0.051 | AB | Availability likely | — |
| Trazodone Hydrochloride 100 mg 68382-0610-01 | Zydus | 100 tablets | $0.051 | AB | Availability likely | — |
| Trazodone Hydrochloride 100 mg 68382-0806-01 | Zydus | 100 tablets | $0.051 | AB | Availability likely | — |
| Trazodone Hydrochloride 100 mg 70010-0232-01 | Granules | 100 tablets | $0.051 | AB | Availability likely | — |
| Trazodone Hydrochloride 100 mg 00615-8386-05 | NCS | 15 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 42291-0869-10 | AvKARE | 1000 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 45865-0505-60 | Medsource | 60 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 50090-4283-00 | A-S | 30 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 50090-6723-00 | A-S | 90 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 51407-0947-01 | Golden | 100 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 51655-0986-26 | Northwind | 90 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 55154-8085-00 | Cardinal | 10 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 60505-2654-00 | Apotex | 100 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 60760-0806-30 | St. | 30 tablets | — | AB | Discontinued | — |
| Trazodone Hydrochloride 100 mg 67046-1540-03 | Coupler | 30 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 67046-1662-03 | Coupler | 30 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 68071-2959-03 | NuCare | 30 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 68071-4761-03 | NuCare | 30 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 68071-4833-01 | NuCare | 100 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 68788-7137-01 | Preferred | 100 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 69584-0885-10 | Oxford | 100 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 70518-1204-02 | REMEDYREPACK | 30 tablets | — | AB | Discontinued | — |
| Trazodone Hydrochloride 100 mg 70518-2973-00 | REMEDYREPACK | 30 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 70518-3403-00 | REMEDYREPACK | 100 tablets | — | AB | Discontinued | — |
| Trazodone Hydrochloride 100 mg 70518-3426-00 | REMEDYREPACK | 30 tablets | — | AB | Discontinued | — |
| Trazodone Hydrochloride 100 mg 70518-3756-00 | REMEDYREPACK | 30 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 70771-1129-00 | Zydus | 1000 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 70771-1939-00 | Zydus | 1000 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 71205-0574-30 | Proficient | 30 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 71205-0630-30 | Proficient | 30 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 71335-0730-01 | Bryant | 30 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 71335-3022-02 | Bryant | 30 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 71335-3023-01 | Bryant | 500 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 71335-3041-01 | Bryant | 100 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 71335-3098-01 | Bryant | 30 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 71610-0511-30 | Aphena | 30 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 71610-0513-30 | Aphena | 30 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 71610-0530-30 | Aphena | 30 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 71610-0537-30 | Aphena | 30 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 72162-2531-00 | Bryant | 1000 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mgthis 72789-0168-30 | PD-Rx | 30 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 72789-0424-30 | PD-Rx | 30 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 76420-0648-01 | Asclemed | 100 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 80425-0298-01 | Advanced | 30 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 71335-1630-01 | Bryant | 30 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 87441-0080-01 | Unit | 30 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 72789-0588-90 | PD-Rx | 90 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 70518-4737-00 | REMEDYREPACK | 90 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 50090-8080-00 | A-S | 30 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 50090-8077-00 | A-S | 1000 tablets | — | AB | FDA listed | — |
| Trazodone Hydrochloride 100 mg 87063-0321-01 | ASCLEMED | 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 8, 2026
- FDA Orange Book · refreshed Oct 3, 2026
- CMS NADAC weekly file
Availability & generic status
🏛️
2017
On the market since
Dec 2017
📍
2026
Currently FDA-listed
9 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.
- FDA Orange Book · refreshed Oct 3, 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.
🧪 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.
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 6, 2026
- FDA openFDA NDC Directory · synced Oct 8, 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
LabelerPD-Rx Pharmaceuticals, Inc.
Application holderZYDUS PHARMACEUTICALS USA INC
FDA applicationANDA205253 (ANDA)
Labeler code72789
First marketedDec 2017
Product typeHuman Prescription Drug
Portfolio835 products on file
More NDCs from PD-Rx Pharmaceuticals, Inc. labeler code 72789
- Losartan Potassium and Hydrochlorothiazide 50 mg; 12.5 mg Tablet, Film Coated NDC 72789-162-30
- Losartan Potassium 25 mg 25 mg Tablet, Film Coated NDC 72789-163-90
- Losartan Potassium 50 mg 50 mg Tablet, Film Coated NDC 72789-164-90
- Losartan Potassium 100 mg 100 mg Tablet, Film Coated NDC 72789-165-90
- Docusate Sodium 250 mg Capsule, Liquid Filled NDC 72789-166-60
- Clindamycin Hydrochloride 300 mg Capsule NDC 72789-167-09
- Lithium Carbonate 300 mg Tablet, Extended Release NDC 72789-171-01
- Lithium Carbonate 600 mg Capsule, Gelatin Coated NDC 72789-172-01
- Lithium Carbonate 300 mg Capsule, Gelatin Coated NDC 72789-173-01
- Lithium Carbonate 300 mg Tablet NDC 72789-174-01
- Hydrochlorothiazide 12.5 mg Capsule NDC 72789-176-06
- Primidone 250 mg Tablet NDC 72789-177-01
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 8, 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.
📄 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 ↗
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 | — Not published for this NDC No photo available yet for this listing. |
| 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 it is currently marketed — but PD-Rx Pharmaceuticals, Inc. has reported a marketing end date of 2027-02-28, after which this package is expected to stop being marketed. The directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 90 tablets (72789-0168-90). 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?
PD-Rx Pharmaceuticals, 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.
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.