![First Aid Antibiotic BACITRACIN ZINC 500 [USP'U]/g Ointment — NDC 11673-0790-14 package photo](https://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=6020956d-2f58-4be8-97da-3f6b7e0f34aa&name=591020+Carton.jpg)
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.
First Aid Antibiotic BACITRACIN ZINC 500 [USP'U]/g Ointment — NDC 11673-790-14 (Billing 11673-0790-14)
by Target Corporation · 1 TUBE in 1 CARTON (11673-790-14) / 14 g in 1 TUBE
NDC 11673-790-14 (billing 11673-0790-14) is a package of First Aid Antibiotic BACITRACIN ZINC 500 [USP'U]/g Ointment from Target Corporation, marketed since Jan 2024 and currently FDA-listed. It is this product's only package size.
NDC 11673-0790-14
🏷️ FDA NDC (as labeled)
11673-790-14
billing pads the product segment with a zero
🗂️ 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 →
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
FDA NDC (as labeled)
11673-790-14
Product NDC
11673-790
11-digit billing NDC
11673079014
RxCUI
1366116
UNII
89Y4M234ES
Application #
M004
SPL Set ID
6020956d-2f58-4be8-97da-3f6b7e0f34aa
Physiologic effect
Decreased Cell Wall Synthesis & Repair
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2024-01-31
Route
TOPICAL
Dosage form
OINTMENT
Substance
BACITRACIN ZINC
Quick answers for NDC 11673-790-14
- RxCUI (RxNorm): 1366116
- 11-digit billing NDC: 11673079014
Why two NDCs?
The FDA registers this code as 11673-790-14 — 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 → 11673-0790-14. 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 Sep 24, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 1, 2026
RxNorm drug class
This medicine belongs to the Other antibiotics for topical use class.
Drug family (ATC)
Other antibiotics for topical use, Other antibacterials, Antibiotics
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 Sep 24, 2026
Clinical
📖 What it is MedlinePlus · NLM
Bacitracin is used to help prevent minor skin injuries such as cuts, scrapes, and burns from becoming infected. Bacitracin is in a class of medications called antibiotics. Bacitracin works by stopping the growth of bacteria.
Read the full MedlinePlus article ↗📗 Our plain-language guide HelloPharmacist
- It is first aid to help prevent infection in minor cuts, scrapes, and burns. One cream product also has directions for athlete's foot, ringworm and jock itch.
- Clean the area, then put on a small amount, about the size of your fingertip. Do this 1 to 3 times a day, and you can cover it with a sterile bandage. One cream product is used as...
- Not longer than 1 week unless a doctor tells you to. If the problem is not getting better or gets worse, stop and check with a doctor.
- Stop if you get a rash or any allergic reaction, and talk to a doctor. Don't use it if you are allergic to any ingredient.
Patient education
Supplement & herbal interactions
7
Nutrient depletion considerations
Bacitracin may be associated with lower levels of 7 nutrients — worth a chat with your pharmacist, not a cause for alarm.
BIOTIN
Insignificant Depletion
FOLIC ACID
Insignificant Depletion
RIBOFLAVIN
Insignificant Depletion
THIAMINE
Insignificant Depletion
VITAMIN B12
Insignificant Depletion
+2 more
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 BACITRACIN ZINC?
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 g | 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 1, 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 |
|---|---|---|---|---|
| 11673-0790-14 11673-790-14 You're viewing this Main listing | 1 TUBE in 1 CARTON (11673-790-14) / 14 g in 1 TUBE | 2024-01-31 | — | Active |
Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Bacitracin Zinc 500 [USP'U]/g 00536-1263-28 | Rugby | 1 tube | $0.074 | — | Availability likely | — |
| Leader Bacitracin Zinc 500 [USP'U]/g 70000-0547-01 | Cardinal | 1 tube | $0.074 | — | Availability likely | — |
| Good Neighbor Pharmacy Bacitracin Zinc 500 [iU]/g 24385-0060-03 | AmerisourceBergen | 1 tube | $0.093 | — | Availability likely | — |
| Bacitracin Zinc 500 [USP'U]/g 70677-1211-01 | STRATEGIC | 1 tube | $0.093 | — | Availability likely | — |
| antibiotic Bacitracin Zinc 500 [iU]/g 49348-0154-72 | Strategic | 1 tube | $0.095 | — | Discontinued | — |
| Bacitracin Zinc 500 [USP'U]/g 51672-2075-01 | Sun | 1 tube | $0.186 | — | Availability likely | — |
| Bacitracin Zinc 500 [USP'U]/g 68001-0531-45 | BluePoint | 1 tube | $0.186 | — | Availability likely | — |
| Bacitracin Zinc 500 [iU]/g 00404-0170-50 | Henry | 1 tube | — | — | FDA listed | — |
| Bacitracin Zinc 500 [iU]/g 00404-0172-50 | Henry | 144 packets | — | — | FDA listed | — |
| Major Bacitracin 500 [USP'U]/g 00904-7023-67 | Major | 144 packets | — | — | FDA listed | — |
| Sheffield Bacitracin Zinc 500 [USP'U]/g 11527-0163-15 | Sheffield | 1 tube | — | — | FDA listed | — |
| First Aid Antibiotic 500 [USP'U]/g 11673-0396-01 | TARGET | 1 tube | — | — | FDA listed | — |
| First Aid Antibiotic 500 [USP'U]/gthis 11673-0790-14 | Target | 1 tube | — | — | FDA listed | — |
| Bacitracin Zinc 500 [USP'U]/g 21922-0091-04 | Encube | 1 tube | — | — | FDA listed | — |
| TopCare Bacitracin Zinc 500 [iU]/g 36800-0089-02 | Topco | 1 tube | — | — | FDA listed | — |
| Medi-First Bacitracin Zinc 500 [USP'U]/g 47682-0863-66 | Unifirst | 1 tube | — | — | FDA listed | — |
| Bacitracin Zinc 500 [USP'U]/g 49035-0510-26 | EQUATE | 1 tube | — | — | Discontinued | — |
| Bacitracin Zinc 500 [USP'U]/g 50090-4706-00 | A-S | 1 tube | — | — | FDA listed | — |
| Live Better Bacitracin Zinc 500 [iU]/g 51143-0075-02 | The | 1 tube | — | — | FDA listed | — |
| CAREALL Bacitracin 500 [USP'U]/g 51824-0003-01 | New | 28 g | — | — | FDA listed | — |
| Bacitracin Zinc 500 [USP'U]/g 52000-0059-01 | Universal | 1 tube | — | — | Discontinued | — |
| Medpride First Aid 500 [USP'U]/g 52410-3035-02 | Shield | 9 g | — | — | FDA listed | — |
| First Aid Antibiotic 500 [USP'U]/g 53329-0089-01 | Medline | 1 tube | — | — | FDA listed | — |
| ProCure Bacitracin Zinc 500 [iU]/g 55681-0016-01 | Twin | 28.3 g | — | — | FDA listed | — |
| procureFirst Aid Antibio First Aid Antibiotic 500 U/g 55681-0218-01 | TWIN | 9 g | — | — | FDA listed | — |
| Bacitracin Zinc 500 [USP'U]/g 57896-0145-14 | Geri-Care | 144 packets | — | — | FDA listed | — |
| Bacitracin Zinc 500 [USP'U]/g 58980-0011-01 | STRATUS | 144 packets | — | — | FDA listed | — |
| Bacitracin 500 [iU]/g 59898-0720-01 | Water-Jel | 1728 packets | — | — | FDA listed | — |
| Single Antibiotic 500 [iU]/g 61010-4404-01 | Safetec | 28.4 g | — | — | FDA listed | — |
| Family Care First Aid 500 [USP'U]/g 65923-0491-33 | United | 1 tube | — | — | FDA listed | — |
| Winco Bacitracin Zinc 500 [USP'U]/g 67091-0270-28 | WinCo | 1 tube | — | — | FDA listed | — |
| Bacitracin Zinc 500 [USP'U]/g 67777-0008-10 | Dynarex | 144 packets | — | — | FDA listed | — |
| Premier Value Bacitracin Zinc 500 [USP'U]/g 68016-0107-01 | Pharmacy | 1 tube | — | — | FDA listed | — |
| Sion Biotext Bacitracin Zinc 500 [iU]/g 68786-0500-01 | Sion | 28 g | — | — | FDA listed | — |
| Bacitracin 500 [USP'U]/g 69396-0027-01 | Trifecta | 1 tube | — | — | FDA listed | — |
| Bacitracin Zinc 500 [USP'U]/g 69396-0098-09 | Trifecta | 144 packets | — | — | FDA listed | — |
| Bacitracin Zinc 500 [USP'U]/g 69396-0104-09 | Trifecta | 144 packets | — | — | FDA listed | — |
| Always Save Bacitracin Zinc 500 [USP'U]/g 69396-0148-01 | Trifecta | 1 tube | — | — | FDA listed | — |
| Bacitracin Zinc 500 [USP'U]/g 69396-0163-09 | Trifecta | 144 packets | — | — | FDA listed | — |
| FifthPulse Bacitracin Zinc 4oz 500 [iU]/g 69571-0012-02 | Front | 113.4 g | — | — | FDA listed | — |
| FifthPulse Bacitracin Zinc 1oz 500 [iU]/g 69571-0013-01 | Front | 28.4 g | — | — | FDA listed | — |
| Gerigentle-Bacitracin zinc 500 [USP'U]/g 69771-0106-34 | Geri-Gentle | 144 packets | — | — | FDA listed | — |
| Vitastem ULTRA 500 U/mL 71262-0007-15 | ViaDerma | 1 bottle | — | — | FDA listed | — |
| Equate 500 [USP'U]/g 79903-0372-01 | Walmart | 1 tube | — | — | FDA listed | — |
| Drs. Antibiotic Bacitracin 500 [USP'U]/g 80489-0006-01 | OL | 1 tube | — | — | FDA listed | — |
| Bacitracin Zinc 500 [USP'U]/g 83324-0040-01 | Chain | 1 tube | — | — | FDA listed | — |
| ElixirBaciShield First Aid 500 [USP'U]/g 84546-0002-01 | ELIXIR | 28.3 g | — | — | FDA listed | — |
| Bacitracin Zinc 500 [USP'U]/g 87236-0001-01 | Aldermed | 1 tube | — | — | FDA listed | — |
| FifthPulse Bacitracin Zinc 500 U/g 87525-0001-01 | WeCare | 1 tube | — | — | FDA listed | — |
| Publix Bacitracin Zinc 500 [USP'U]/g 56062-0815-28 | PUBLIX | 1 tube | — | — | FDA listed | — |
| astonea First Aid 500 [USP'U]/g 77338-0303-52 | ASTONEA | 9 g | — | — | FDA listed | — |
| Bacitracin 500 [USP'U]/g 68788-4153-02 | Preferred | 1 tube | — | — | FDA listed | — |
| CAREALL Bacitracin 500 [USP'U]/g 51824-0116-01 | New | 28 g | — | — | FDA listed | — |
| Dealmed Bacitracin 500 [USP'U]/g 70082-0016-01 | Dealmed | 144 packets | — | — | 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.
- 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
Jan 2024
📍
2026
Currently FDA-listed
2 years listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found
We did not find an FDA-approved generic match for this exact strength, form and route.
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
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 4T6H12BN9U
Petrolatum is a purified mineral oil-based jelly derived from petroleum. In medicines, it acts as an emollient, lubricant, and moisture barrier to soften skin, reduce friction, and help prevent water loss from formulations.
1 inactive ingredient listed in the exact product block matched to this NDC.
The official label also statesPetrolatum
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.- 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
LabelerTarget Corporation
FDA applicationM004 (OTC MONOGRAPH DRUG)
Labeler code11673
First marketedJan 2024
Product typeHuman Otc Drug
Portfolio409 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
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
⏱️ Dosage and Administration
⚠️ Warnings
🧪 Active Ingredient
🧪 Inactive Ingredients
🎯 Purpose
📄 Stop Use and Ask a Doctor If
📄 Keep Out of Reach of Children
📄 Other Information
📄 Questions or Comments
📄 Package Label / Principal Display Panel
🎯 Indications and Usage ▾
Uses First aid to help prevent infection in minor: cuts scrapes burns
⏱️ Dosage and Administration ▾
Directions clean the affected area apply a small amount (equal to surface area of tip of finger) on the area 1 to 3 times daily. may be covered with a sterile bandage
⚠️ Warnings ▾
Warnings For external use only Allergy alert do not use if you are allergic to any of the ingredients Do not use in or near eyes on large arteas of the body Consult a doctor before use if you have deep puncture wounds animal bites serious burns When using this product do not use longer than 1 week
🧪 Active Ingredient ▾
Active Ingredient Bacitracin 500 units
🧪 Inactive Ingredients ▾
Inactive ingredient Petrolatum
🎯 Purpose ▾
Uses Bacitracin -First Aid Antibiotic
📄 Stop Use and Ask a Doctor If ▾
Stop use and consult a doctor if condition persists or gets worse symptoms last for more than 7 days or clear up and come back within a few days a rash or other allergic reaction develops
📄 Keep Out of Reach of Children ▾
Keep out of the reach of children If swallowed get medical help or contact a Poison Control Center immediately.
📄 Other Information ▾
Other information Store at a controlled room temperature 20º-25ºC (68° to 77°F)
📄 Questions or Comments ▾
Questions? 1-800-910-6874
📄 Package Label / Principal Display Panel ▾
Principal Display Panel Target Up and Up NDC 11673-790-14 Bacitracin ointment First aid Antibiotic Ointment NET WT 0.5OZ (14g) 291020 Tube 591020 Carton
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 ↗
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 First Aid Antibiotic (this brand).
Top reported reactions
Age at onset
Reporter sex
Male · 40%
Female · 59%
Unknown · 0%
Serious outcomes
Reports over time (by year) — tap or hover for the count & year
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 11673-790-14, 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: 11673-0790-14, written without dashes as 11673079014. 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 11673-0790-14, the first segment (11673) is the labeler code FDA assigned to Target Corporation; the middle segment (0790) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (14) 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 Target Corporation. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Target Corporation 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.
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.