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Minoxidil Hair Regrowth Treatment 5 g/100mL Liquid, 100 mL — NDC 85636-0033-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Minoxidil Hair Regrowth Treatment 5 g/100mL Liquid, 100 mL — NDC 85636-033-01 (Billing 85636-0033-01) · Product 85636-033

by Shenzhen Earth Surface Trading Co., Ltd. · 100 mL in 1 BOTTLE (85636-033-01)

NDC 85636-033-01 (billing 85636-0033-01) is a package of 100 mL of Minoxidil Hair Regrowth Treatment 5 g/100mL Liquid from Shenzhen Earth Surface Trading Co., Ltd., marketed since May 2026 and currently FDA-listed. It is the main listing for product NDC 85636-033, its only package size.

NDC 85636-0033-01
🏷️ FDA NDC (as labeled) 85636-033-01 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Sep 10, 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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 85636-033-01
Product NDC 85636-033
11-digit billing NDC 85636003301
RxCUI 1537948
UNII 5965120SH1
Application # M032
SPL Set ID 59b67ce0-3546-c18a-e063-6394a90ae50a
Established class (EPC) Arteriolar Vasodilator
Physiologic effect Arteriolar Vasodilation
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-05-01
Route TOPICAL
Dosage form LIQUID
Substance MINOXIDIL
Quick answers for NDC 85636-033-01
  • RxCUI (RxNorm): 1537948
  • 11-digit billing NDC: 85636003301
Why two NDCs? The FDA registers this code as 85636-033-01 — 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 → 85636-0033-01. 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.

RxNorm drug class

This medicine belongs to the Arteriolar Vasodilator class.

Pharmacologic class Arteriolar Vasodilator
Drug family (ATC) Pyrimidine derivatives, Other dermatologicals
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.

Clinical

📗 Our plain-language guide HelloPharmacist
  • The topical products in the label are specifically approved for hair regrowth on the top of the scalp only — not for use on other parts of the body. Applying it elsewhere isn't rec...
  • Can I use the topical minoxidil solution on my beard or other areas, not just my scalp?
  • Hair regrowth takes time and patience. Some people start to see results after about 2 months of twice-daily use, but for others it may take 4 months or more. Not everyone responds...
  • How long does it take to see results with topical minoxidil?
📖 Read our full Minoxidil guide →
1
Nutrient depletion considerations

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

🧪 Full Minoxidil 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 mLPer 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
85636-0033-01 85636-033-01 You're viewing this Main listing 100 mL in 1 BOTTLE (85636-033-01) 2026-05-01 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Leader Minoxidil 5 g/100mL 70000-0653-01 Cardinal 3 bottles $0.301 — Availability likely —
equate hair regrowth treatment 5 g/100mL 49035-0746-16 Wal-Mart 1 bottle — — FDA listed —
Elevate Hair Growth Serum 5 g/100mL 81653-0010-01 Guangzhou 60 ml — — FDA listed —
Minoxidil Hair Regrowth Treatment 5 g/100mL 85636-0024-01 Shenzhen 60 ml — — FDA listed —
Hair regrowth treatment 5 g/100mL 81653-0005-01 Guangzhou 3 bottles — — FDA listed —
Minoxidil Hair Growth Serum 5 g/100mL 85092-0001-01 Shenzhen 1 bottle — — Discontinued —
5% MINOXIDIL TOPICAL Solution 5 g/100mL 85174-0001-02 Nanhong 2 bottles — — Discontinued —
5% Minoxidil Hair Regrowth Treatment 5 g/100mL 85636-0023-01 Shenzhen 60 ml — — FDA listed —
hims hair regrowth treatment 5 g/100mL 71730-0000-16 Hims 1 bottle — — FDA listed —
Hair Beardgrowth Foam 5 g/100mL 85173-0001-01 Shenzhen 60 ml — — FDA listed —
Good Sense Hair Regrowth Treatment 5 g/100mL 00113-1032-30 L. 3 bottles — — FDA listed —
hair regrowth treatment 5 g/100mL 00363-0032-16 Walgreen 1 bottle — — FDA listed —
equate hair regrowth treatment 5 g/100mL 79903-0222-01 WALMART 1 bottle — — FDA listed —
minoxidil 5 g/100mL 56062-0322-16 Publix 1 bottle — — FDA listed —
hair regrowth treatment 5 g/100mL 41250-0428-30 Meijer, 3 bottles — — FDA listed —
kirkland signature minoxidil 5 g/100mL 63981-0032-40 Costco 6 bottles — — FDA listed —
hair regrowth treatment 5 g/100mL 11822-1260-00 Rite 1 bottle — — FDA listed —
hair regrowth treatment 5 g/100mL 30142-0632-30 Kroger 3 bottles — — FDA listed —
Soti Hair Growth Serum 5 g/100mL 81653-0013-01 Guangzhou 60 ml — — FDA listed —
minoxidil 5 g/100mL 37808-0833-16 H 1 bottle — — FDA listed —
members mark hair regrowth treatment 5 g/100mL 68196-0032-40 Sam's 6 bottles — — FDA listed —
OLIVITA Minoxidil 5 g/100mL 83818-0031-01 Shenzhen 60 ml — — FDA listed —
Hair Regen Hair Growth Treatment 5 g/100mL 84232-0001-01 YIWUYIZHOUTRADINGCO.,LTD 60 ml — — FDA listed —
Minoxidil Hair Growth Serum 5 g/100mL 85741-0004-01 Shenzhen 1 bottle — — FDA listed —
hair regrowth treatment 5 g/100mL 21130-0611-16 Safeway 1 bottle — — FDA listed —
signature care hair regrowth treatment 5 g/100mL 21130-0819-16 Safeway 1 bottle — — Discontinued —
minoxidil 5 g/100mL 71713-0094-16 THIRTY 1 bottle — — FDA listed —
Minoxidil Extra Strength for Men 5 g/100mL 72484-0095-03 Roman 1 bottle — — FDA listed —
VENANOCI Minoxidil 5 g/100mL 83818-0029-01 Shenzhen 60 ml — — FDA listed —
Hair-Regen Hair Growth Treatment 5 g/100mL 84232-0011-26 Yiwu 6 bottles — — FDA listed —
Hair Growth Serum Roll-ON 5 g/100mL 85524-2625-02 FlexiGo 1 bottle — — FDA listed —
LILIVERA Hair Regrowth Kit 5 g/100mL 60771-0012-01 Guangzhou 60 ml — — FDA listed —
basic care hair regrowth treatment 5 g/100mL 72288-0798-16 Amazon.com 60 ml — — FDA listed —
up and up hair regrowth treatment for men 5 g/100mL 11673-0317-30 Target 3 bottles — — FDA listed —
Psalmonica Hair Growth Serum 5 g/100mL 60771-0013-01 Guangzhou 60 ml — — FDA listed —
Hair Regrowth Treatment 5 g/100mL 69842-0598-16 CVS 1 bottle — — FDA listed —
5%Minoxidil Hair Growth Serum 5 g/100mL 84355-0003-01 Guangzhou 1 bottle — — FDA listed —
5%Minoxidil Hair Growth Sprays Serum 5 g/100mL 84355-0004-01 Guangzhou 1 bottle — — FDA listed —
Minoxidil Hair Regrowth Treatment 5 g/100mL 85636-0031-01 Shenzhen 100 ml — — FDA listed —
Minoxidil Hair Regrowth Treatment 5 g/100mL 85636-0032-01 Shenzhen 60 ml — — FDA listed —
Minoxidil Hair Regrowth Treatment 5 g/100mLthis 85636-0033-01 Shenzhen 100 ml — — FDA listed —
ValBello 5 g/100mL 87942-0001-01 ValBello 125 ml — — FDA listed —
Hair Regrowth Treatment 5 g/100mL 72288-0667-40 Amazon.com 6 bottles — — FDA listed —
Minoxidil Extra Strength (For Men) 5 g/100mL 85524-2615-02 FlexiGo 1 bottle — — FDA listed —
Minoxidil Extra Strength (For Men) 5 g/100mL 85524-2614-02 FlexiGo 1 bottle — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
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
May 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔓
·
Generic versions listed
see equivalents
✅Generic appears available

FDA-approved generic versions are listed, and recent pricing/market data suggests they may be available — see Therapeutic equivalents.

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.

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 6SO6U10H04
    Biotin is a B-vitamin used as a nutritional supplement in some medications. It may also serve as a colorant or marker in formulations.
  • UNII 3G6A5W338E
    Caffeine is a natural stimulant compound commonly extracted from coffee beans and tea leaves. In medicines, it serves as an active booster in pain relievers and cold products to enhance alertness and improve the effectiveness of other ingredients.
  • UNII D5340Y2I9G
    Castor oil is a natural plant-based oil used in medicines as a lubricant, laxative agent, and solvent. It helps medicine ingredients dissolve or flow smoothly and can aid bowel movement in formulations designed for that purpose.
  • UNII FGL3685T2X
    Chamomile is a plant extract used in medications as a flavoring agent and for its mild soothing properties in formulations. It helps improve taste and aroma of the medicine.
  • UNII 06JMS448M5
    A plant extract from lemongrass leaves used in medicines as a flavoring agent and fragrance component. It adds taste and aroma to make the product more pleasant to take.
  • UNII C5529G5JPQ
    Ginger is a plant-derived ingredient used as a flavoring agent to add taste and aroma to medicines. It may also provide mild soothing properties to support product palatability.
  • UNII ZBP1YXW0H8
    A fragrant oil extracted from lavender plants, used as a flavoring and scent agent in medicines to improve taste and aroma.
  • UNII 1VPU26JZZ4
    Potassium sorbate is a salt derived from sorbic acid, a naturally occurring preservative. It prevents growth of mold, yeast, and some bacteria, extending the medicine's shelf life.
  • UNII 6DC9Q167V3
    Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
  • UNII IJ67X351P9
    A natural plant extract from rosemary leaves used as a preservative to help prevent oils and fats in the medicine from spoiling or becoming rancid during storage.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.

11 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesWater, Propylene Glycol, Potassium Sorbate, Castor Oil, Lavender Oil, Cymbopogon Citratus Leaf, Chamomile, Biotin, Rosemary Oil, Ginger, Batana Oil, Caffeine

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

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

LabelerShenzhen Earth Surface Trading Co., Ltd.
FDA applicationM032 (OTC MONOGRAPH DRUG)
Labeler code85636
First marketedMay 2026
Product typeHuman Otc Drug
Portfolio31 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 label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📋 Description 📄 Do Not Use 📄 Ask a Doctor Before Use If 📄 When Using This Product 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 15 words ▾

Use Use to regrow hair of the scalp and beard growth for men and wemen

⚠️ Warnings 12 words ▾

Warnings Warnings For external use only. Keep out of reach of children.

🧪 Active Ingredient 5 words ▾

ACTIVE INGREDIENT Minoxidil 5% w/w

🧪 Inactive Ingredients 23 words ▾

Inactive ingredients Water, Propylene Glycol, Potassium Sorbate, Castor Oil, Lavender Oil, Cymbopogon Citratus Leaf, Chamomile, Biotin , Rosemary Oil, Ginger, Batana Oil, Caffeine

🎯 Purpose 3 words ▾

Purpose Hair Regrowth

📋 Description 54 words ▾

Directions Directions Apply twice a day. Once in the morning and another time in the evening before bed Spray directly on top of the scalp in the area to be treated Using more than directed or more often will not improve results Continued use is necessary to lncrease and then malntain your hair regrowth

📄 Do Not Use 70 words ▾

Do not use if Do not use if You have no family history of hair loss. Your hair loss is sudden and/or patchy. Your hair loss is associated with childbirth. You do not know the reason for your hair loss. You are under 18 years of age. Do not use on babies and children. Your scalp is red, inflamed, infected, irritated, or painful. You use other medicines on the scalp.

📄 Ask a Doctor Before Use If 50 words ▾

Stop Use And Ask A Doctor Stop Use And Ask A Doctor Chest pain, rapid heartbeat, faintness, or dizziness occurs. Sudden, unexplained weight gain occurs. Scalp irritation or redness occurs. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

📄 When Using This Product 23 words ▾

When Using When Using Avoid contact with eyes. In case of accidental contact, rinse eyes with a large amount of cool tap water.

📄 Keep Out of Reach of Children 12 words ▾

Keep Out Of Reach Of Children Keep Out Of Reach Of Children

📄 Questions or Comments 41 words ▾

Other information Other information Before use, read all information on carton and enclosed leaflet. Store at controlled room temperature 10° to 30°C (50° to 80°F). Do not incinerate container. Do not expose to heat or store at temperature above 104°F (40°C).

📄 Package Label / Principal Display Panel 2 words ▾

LABEL 01

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

Medicare Part D spend CMS · PART D · 2026 (Q1)

Medicare Part D (outpatient prescription) spending for Minoxidil (matched by generic name) — the program that covers self-administered drugs. 3 manufacturers.
⚠️ Drug-level data: CMS publishes Part D spending by drug, not by NDC — these figures combine every manufacturer, strength and package size sold under the name Minoxidil. That’s a different level of aggregation than the Medicaid card above, which is specific to this exact 11-digit NDC (pack size included), so the two aren’t directly comparable.
Period
Total Part D spend
$3.5M
Claims incl. refills
260.9K
Beneficiaries
202.1K
Spend / beneficiary
$17.33
Spend / claim
$13.42
Trend by period
💵 About the dollar figures: spending is what Part D plans paid before confidential manufacturer rebates, so the program’s real net cost is lower. A blank patient count means fewer than 11 people — CMS hides counts that small to protect privacy. Source: CMS Medicare Quarterly Part D Spending by Drug (data.cms.gov), updated quarterly.

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 Minoxidil Hair Regrowth Treatment (this brand).

Top reported reactions

Adverse Drug Reaction8,573
Application Site Pruritus2,535
Application Site Irritation1,229
Application Site Pain1,091
Headache1,080
Alopecia884
Application Site Dryness738

Age at onset

Neonate3
Infant14
Child12
Adolescent16
Adult1,717
Elderly377

Reporter sex

32,799 reports
Male · 77%
Female · 23%
Unknown · 0%

Serious outcomes

Hospitalization2,046
Death448
Disabling273
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 7,986 0
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.

About this NDC listing & data coverage

Over-the-counter (OTC) 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 — 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

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
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 85636-033-01, 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: 85636-0033-01, written without dashes as 85636003301. 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 85636-0033-01, the first segment (85636) is the labeler code FDA assigned to Shenzhen Earth Surface Trading Co., Ltd.; the middle segment (0033) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) 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 Shenzhen Earth Surface Trading Co., Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Shenzhen Earth Surface Trading Co., Ltd. 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 an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
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.
← 85636-0032-01 · Shenzhen 85636-0034-01 · Shenzhen →
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.