Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.
Dicyclomine hydrochloride 20 mg Tablet, 30-count — NDC 50090-8090-0 (Billing 50090-8090-00)
by A-S Medication Solutions · 30 TABLET in 1 BOTTLE
This is a package of 30 tablets of Dicyclomine hydrochloride 20 mg Tablet from A-S Medication Solutions, marketed since May 2024 and currently FDA-listed. It is the main listing for this product, which comes in 3 package sizes.
NDC 50090-8090-00
🏷️ FDA NDC (as labeled)
50090-8090-0
billing pads the package segment with a zero
This package
Contains30-count
Pack sizes3 compare ↓
Main listing for product 50090-8090 · Also comes in:
20 tablets 50090-8090-2
90 tablets 50090-8090-8
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Oct 2, 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 Dicyclomine Hydrochloride (different manufacturers) — 1 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Jul 23, 2026 — shortfill; reports of empty capsules. (Aurobindo Pharma USA Inc) · FDA recall D-0733-2026
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)
50090-8090-0
Product NDC
50090-8090
11-digit billing NDC
50090809000
Application #
ANDA217566
SPL Set ID
765cc40c-306f-4719-aac1-00f0cd8bbe78
Established class (EPC)
Anticholinergic
Mechanism of action
Cholinergic Antagonists
DEA schedule
Non-controlled
Marketing category
ANDA
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2024-05-07
Route
ORAL
Dosage form
TABLET
Substance
DICYCLOMINE HYDROCHLORIDE
TE code (Orange Book)
AB · RLD · RS
Why two NDCs?
The FDA registers this code as 50090-8090-0 — 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 → 50090-8090-00. 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
Clinical
📗 Our plain-language guide HelloPharmacist
- It treats functional bowel/irritable bowel syndrome. It helps calm the spasms and cramping in your intestines.
- The capsules, tablets and solution are taken by mouth, generally four times a day. Your prescriber may adjust the amount after a week or so. If you miss a dose, just carry on with...
- Dry mouth, dizziness and blurred vision are the most common. Nausea, drowsiness, weakness and nervousness can happen too. Be careful driving until you know how it affects you.
- Call if you feel confused, see or hear things that aren't there, have a racing heartbeat, or can't pass urine. Also call if you overheat without sweating or have diarrhea with a co...
Patient education
Supplement & herbal interactions
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 Dicyclomine 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.
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 |
|---|---|---|---|---|
| 50090-8090-00 You're viewing this Main listing | 30 TABLET in 1 BOTTLE | 2026-09-23 | — | Active |
| 50090-8090-02 50090-8090-2 | 20 TABLET in 1 BOTTLE | 2026-09-23 | — | Active |
| 50090-8090-08 50090-8090-8 | 90 TABLET in 1 BOTTLE | 2026-09-23 | — | Active |
You're viewing one of 3 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.
How does this package differ from NDC 50090-8090-02?
Both are Dicyclomine hydrochloride 20 mg Tablet — the drug itself is identical. This page's package is the 30-count one, while NDC 50090-8090-02 is the 20 tablets package.
What NDC number is used to bill for this package of Dicyclomine hydrochloride 20 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 |
|---|---|---|---|---|---|---|
| Dicyclomine hydrochloride 20 mg 00832-6052-10 | Upsher-Smith | 1000 tablets | $0.056 | AB | Discontinued | — |
| Dicyclomine 20 mg 00143-1227-01 | Hikma | 100 tablets | $0.059 | AB | Availability likely | — |
| Dicyclomine Hydrochloride 20 mg 59651-0720-01 | Aurobindo | 100 tablets | $0.059 | AB | Availability likely | — |
| Dicyclomine Hydrochloride 20 mg 73473-0902-01 | Solaris | 100 tablets | $0.059 | AB | Availability likely | — |
| Dicyclomine hydrochloride 20 mg 16571-0259-01 | Rising | 100 tablets | $0.059 | AB | Availability likely | — |
| Dicyclomine hydrochloride 20 mg 72888-0119-00 | Advagen | 1000 tablets | $0.059 | AB | Availability likely | — |
| Dicyclomine Hydrochloride 20 mg 00591-0795-01 | Actavis | 100 tablets | $0.059 | AB | Availability likely | — |
| Dicyclomine Hydrochloride 20 mg 24979-0200-01 | Upsher-Smith | 100 tablets | $0.059 | AB | Availability likely | — |
| Dicyclomine Hydrochloride 20 mg 62135-0428-12 | Chartwell | 120 tablets | $0.059 | AB | Availability likely | — |
| Dicyclomine hydrochloride 20 mg 31722-0079-01 | Camber | 100 tablets | $0.059 | AB | Availability likely | — |
| Dicyclomine Hydrochloride 20 mg 69452-0311-20 | Bionpharma | 100 tablets | $0.059 | AB | Availability likely | — |
| Dicyclomine Hydrochloride 20 mg 00904-6988-61 | Major | 100 tablets | $0.059 | AB | Availability likely | — |
| Dicyclomine Hydrochloride 20 mg 60687-0380-01 | American | 100 tablets | $0.059 | AB | Availability likely | — |
| Dicyclomine Hydrochloride 20 mg 00527-1282-01 | Lannett | 100 tablets | $0.059 | AB | Availability likely | — |
| Dicyclomine Hydrochloride 20 mg 63187-0784-15 | Proficient | 15 tablets | — | AB | FDA listed | — |
| Dicyclomine Hydrochloride 20 mg 71610-0209-09 | Aphena | 9000 tablets | — | AB | FDA listed | — |
| Dicyclomine Hydrochloride 20 mg 72162-1077-03 | Bryant | 30 tablets | — | AB | FDA listed | — |
| Dicyclomine Hydrochloride 20 mg 82868-0103-30 | Northwind | 30 tablets | — | AB | FDA listed | — |
| Dicyclomine 20 mg 68071-3782-03 | NuCare | 30 tablets | — | AB | FDA listed | — |
| Dicyclomine Hydrochloride 20 mg 70518-3917-00 | REMEDYREPACK | 30 tablets | — | AB | FDA listed | — |
| Dicyclomine Hydrochloride 20 mg 87441-0007-01 | Unit | 30 tablets | — | AB | FDA listed | — |
| Dicyclomine Hydrochloride 20 mg 43063-0045-04 | PD-Rx | 4 tablets | — | AB | FDA listed | — |
| Dicyclomine hydrochloride 20 mg 60760-0802-30 | St. | 30 tablets | — | AB | FDA listed | — |
| Dicyclomine Hydrochloride 20 mg 63187-0410-15 | Proficient | 15 tablets | — | AB | FDA listed | — |
| Dicyclomine Hydrochloride 20 mg 67296-2154-01 | Redpharm | 15 tablets | — | AB | FDA listed | — |
| Dicyclomine Hydrochloride 20 mg 71335-0425-01 | Bryant | 30 tablets | — | AB | FDA listed | — |
| Dicyclomine Hydrochloride 20 mg 71335-2341-01 | Bryant | 30 tablets | — | AB | FDA listed | — |
| Dicyclomine Hydrochloride 20 mg 72162-2612-00 | Bryant | 1000 tablets | — | AB | FDA listed | — |
| Dicyclomine Hydrochloride 20 mg 67046-1164-03 | Coupler | 30 tablets | — | AB | FDA listed | — |
| Dicyclomine Hydrochloride 20 mg 68788-7811-02 | Preferred | 20 tablets | — | AB | FDA listed | — |
| Dicyclomine Hydrochloride 20 mg 68071-3555-03 | NuCare | 30 tablets | — | AB | FDA listed | — |
| Dicyclomine Hydrochloride 20 mg 68071-3645-03 | NuCare | 30 tablets | — | AB | FDA listed | — |
| Dicyclomine hydrochloride 20 mg 68071-3916-06 | NuCare | 6 tablets | — | AB | FDA listed | — |
| Dicyclomine Hydrochloride 20 mg 68071-3648-06 | NuCare | 100 tablets | — | AB | FDA listed | — |
| Dicyclomine Hydrochloride 20 mg 68788-8751-02 | Preferred | 20 tablets | — | AB | FDA listed | — |
| Dicyclomine Hydrochloride 20 mg 71335-2506-00 | Bryant | 10 tablets | — | AB | FDA listed | — |
| Dicyclomine hydrochloride 20 mg 68071-3885-02 | NuCare | 20 tablets | — | AB | FDA listed | — |
| Dicyclomine hydrochloride 20 mg 68071-5298-03 | NuCare | 30 tablets | — | AB | FDA listed | — |
| Dicyclomine Hydrochloride 20 mg 70518-4393-00 | REMEDYREPACK | 30 tablets | — | AB | FDA listed | — |
| Dicyclomine hydrochloride 20 mg 00615-8622-39 | NCS | 30 tablets | — | AB | FDA listed | — |
| Dicyclomine hydrochloride 20 mg 50090-7732-00 | A-S | 30 tablets | — | AB | FDA listed | — |
| Dicyclomine Hydrochloride 20 mg 50090-7882-00 | A-S | 30 tablets | — | AB | FDA listed | — |
| Dicyclomine Hydrochloride 20 mg 51407-0821-12 | Golden | 120 tablets | — | AB | FDA listed | — |
| Dicyclomine Hydrochloride 20 mg 51655-0257-26 | Northwind | 90 tablets | — | AB | FDA listed | — |
| Dicyclomine Hydrochloride 20 mg 51655-0940-26 | Northwind | 90 tablets | — | AB | FDA listed | — |
| Dicyclomine Hydrochloride 20 mg 60760-0665-30 | St. | 30 tablets | — | AB | FDA listed | — |
| Dicyclomine Hydrochloride 20 mg 68071-3255-01 | NuCare | 10 tablets | — | AB | FDA listed | — |
| Dicyclomine Hydrochloride 20 mg 70518-1767-00 | REMEDYREPACK | 30 tablets | — | AB | Discontinued | — |
| Dicyclomine Hydrochloride 20 mg 72789-0539-01 | PD-Rx | 100 tablets | — | AB | FDA listed | — |
| Dicyclomine Hydrochloride 20 mg 60760-0931-30 | St. | 30 tablets | — | AB | FDA listed | — |
| Dicyclomine hydrochloride 20 mg 67296-2175-01 | Redpharm | 10 tablets | — | AB | FDA listed | — |
| Dicyclomine Hydrochloride 20 mg 67296-2226-05 | Bionpharma | 56 tablets | — | AB | Discontinued | — |
| Dicyclomine hydrochloride 20 mg 72789-0466-01 | PD-Rx | 100 tablets | — | AB | FDA listed | — |
| Dicyclomine Hydrochloride 20 mg 50090-1577-00 | A-S | 30 tablets | — | AB | FDA listed | — |
| Dicyclomine hydrochloride 20 mg 51655-0548-26 | Northwind | 90 tablets | — | AB | FDA listed | — |
| Dicyclomine Hydrochloride 20 mg 68071-3606-06 | NuCare | 6 tablets | — | AB | FDA listed | — |
| Dicyclomine Hydrochloride 20 mg 68071-4782-01 | NuCare | 10 tablets | — | AB | FDA listed | — |
| Dicyclomine Hydrochloride 20 mg 50090-7309-00 | A-S | 30 tablets | — | AB | FDA listed | — |
| Dicyclomine hydrochloride 20 mg 67296-2142-01 | Redpharm | 10 tablets | — | AB | FDA listed | — |
| Dicyclomine hydrochloride 20 mg 70518-4555-00 | REMEDYREPACK | 180 tablets | — | AB | FDA listed | — |
| Dicyclomine hydrochloride 20 mg 71335-2226-01 | Bryant | 30 tablets | — | AB | FDA listed | — |
| Dicyclomine Hydrochloride 20 mg 67296-2294-04 | Redpharm | 15 tablets | — | AB | FDA listed | — |
| Dicyclomine hydrochloride 20 mg 68788-4146-03 | Preferred | 30 tablets | — | AB | FDA listed | — |
| Dicyclomine hydrochloride 20 mg 67296-2311-02 | Redpharm | 15 tablets | — | AB | FDA listed | — |
| dicyclomine hydrochloride 20 mg 00054-0885-25 | Hikma | 100 tablets | — | AB | FDA listed | — |
| Dicyclomine hydrochloride 20 mgthis 50090-8090-00 | A-S | 30 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
🏛️
2024
On the market since
May 2024
📍
2026
Currently FDA-listed
2 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 Sep 3, 2026
What it looks like
Color
blue
ShapeRound
ImprintV1;44
Size7 mm
ScoringNot scored
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.
💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.
-
UNII H3R47K3TBD
FD&C Blue No. 1 is a synthetic blue dye approved for use in foods and medicines. It serves as a colorant to give the medication its distinctive appearance and help with product identification.
-
UNII Q8Y7S3B85M
A naturally derived fatty acid used in medicines as a lubricant and binder. It helps pills slide smoothly during manufacturing and holds ingredients together in solid dosage forms.
-
UNII R75537T0T4
Hypromellose 2910 is a plant-derived thickening agent made from cellulose. It serves as a binder that holds tablet ingredients together, a film-coating for pills, and a viscosity controller in liquids.
-
UNII EWQ57Q8I5X
Lactose monohydrate is a natural sugar derived from milk. It serves as a filler and binder in tablets and capsules, helping create the proper size, texture, and consistency of the medicine.
-
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 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.
7 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.- 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
LabelerA-S Medication Solutions
Application holderANNORA PHARMA PRIVATE LTD
FDA applicationANDA217566 (ANDA)
Labeler code50090
First marketedMay 2024
Product typeHuman Prescription Drug
Portfolio2,811 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.
📄 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 | ✓ 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 A-S Medication Solutions. 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 20 tablets (50090-8090-02), 90 tablets (50090-8090-08). 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?
A-S Medication Solutions 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.