HomeNDC LookupIngredientsErgocalciferol › 10888-0140-01
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ERGOCALCIFEROL 1.25 mg Capsule, Liquid Filled, 20,000-count

by Banner Pharmacaps Inc. · 20000 CAPSULE, LIQUID FILLED in 1 CARTON (10888-0140-1)
NDC 10888-0140-01
🏷️ FDA NDC (as labeled) 10888-0140-1 billing pads the package segment with a zero
On market Non-controlled
🗂️ Data synced 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

FDA NDC (as labeled) 10888-0140-1
Product NDC 10888-0140
11-digit billing NDC 10888014001
SPL Set ID 0dcc62b5-4a03-00ef-e063-6294a90a2991
DEA schedule Non-controlled
Marketing category BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2002-06-01
Dosage form CAPSULE, LIQUID FILLED
Substance ERGOCALCIFEROL
Why two NDCs? The FDA registers this code as 10888-0140-1 — a 5-4-1 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the package segment → 10888-0140-01. 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.

🏭 Manufacturer & labeler

LabelerBanner Pharmacaps Inc.
Labeler code10888
First marketedJun 2002
Product typeBulk Ingredient
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.

🩺 Clinical

📗 Our plain-language guide HelloPharmacist
  • It's the same type of vitamin D (vitamin D2), but at much higher doses. The over-the-counter supplements you see on store shelves are for general wellness, while this prescription...
  • Is this the same vitamin D I can buy at the pharmacy without a prescription?
  • Because the line between a helpful dose and a harmful one is very narrow with ergocalciferol. Too much vitamin D raises your calcium levels to dangerous heights, which can damage y...
  • Why does my doctor keep ordering blood tests while I'm on this medication?
📖 Read our full Ergocalciferol guide →
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.

🧪 Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

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.

💲 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Ergocalciferol 1.25 mg 62135-0439-90 Chartwell 90 capsules $0.114 AA Availability likely
Vitamin D 1.25 mg 50268-0297-15 AvPAK 50 capsules $0.114 AA Availability likely
Ergocalciferol 1.25 mg 69452-0151-20 Bionpharma 100 capsules $0.114 AA Availability likely
Ergocalciferol 1.25 mg 13668-0757-01 Torrent 100 capsules $0.114 AA Availability likely
Vitamin D 1.25 mg 64380-0737-06 Strides 100 capsules $0.114 AA Availability likely
Ergocalciferol 1.25 mg 43353-0238-03 Aphena 3 capsules AA FDA listed
Vitamin D 1.25 mg 63187-0519-06 Proficient 6 capsules AA FDA listed
Ergocalciferol 1.25 mg 11014-0052-01 Catalent 15000 capsules FDA listed
Ergocalciferol 1.25 mg 68788-4092-01 Preferred 100 capsules AA FDA listed
Vitamin D 1.25 mg 70518-1878-01 REMEDYREPACK 12 capsules AA FDA listed
Ergocalciferol 1.25 mgthis 10888-0140-01 Banner 20000 capsules FDA listed
Ergocalciferol 1.25 mg 68071-2295-01 NuCare 100 capsules AA FDA listed
Ergocalciferol 1.25 mg 43063-0711-12 PD-Rx 12 capsules AA FDA listed
Ergocalciferol 1.25 mg 60760-0152-12 St. 12 capsules AA FDA listed
Ergocalciferol 1.25 mg 63629-2447-01 Bryant 100 capsules AA FDA listed
Ergocalciferol 1.25 mg 68071-1951-02 NuCare 12 capsules AA FDA listed
Vitamin D 1.25 mg 72789-0249-01 PD-Rx 100 capsules AA FDA listed
Ergocalciferol 1.25 mg 71335-0062-00 Bryant 45 capsules AA FDA listed
Vitamin D 1.25 mg 71335-0278-00 Bryant 45 capsules AA FDA listed
Ergocalciferol 1.25 mg 71335-1699-01 Bryant 90 capsules AA FDA listed
Ergocalciferol 1.25 mg 42291-0266-01 AvKARE 100 capsules AA FDA listed
Ergocalciferol 1.25 mg 70518-0177-03 REMEDYREPACK 1 capsule AA Discontinued
Ergocalciferol 1.25 mg 11014-0026-01 Catalent 15000 capsules FDA listed
Ergocalciferol 1.25 mg 71335-2246-01 Bryant 4 capsules AA FDA listed
Vitamin D 1.25 mg 51655-0774-27 Northwind 12 capsules AA FDA listed
Ergocalciferol 1.25 mg 71610-0712-03 Aphena 3 capsules AA FDA listed
Vitamin D 1.25 mg 51407-0700-01 Golden 100 capsules AA FDA listed
Vitamin D 1.25 mg 68788-7627-01 Preferred 100 capsules AA FDA listed
Vitamin D 1.25 mg 71610-0552-04 Aphena 4 capsules AA 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

🏛️
2002
On the market since
Jun 2002
📍
2026
Currently FDA-listed
24 years listed
🔓
·
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.

🔬 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 ERGOCALCIFEROL — the ingredient across all brands.

Top reported reactions

Fatigue37,945
Nausea28,189
Diarrhoea27,097
Headache25,982
Pain24,231
Dyspnoea20,506
Arthralgia20,181

Age at onset

Neonate241
Infant164
Child696
Adolescent974
Adult32,535
Elderly32,898

Reporter sex

382,600 reports
Male · 29%
Female · 71%
Unknown · 0%

Serious outcomes

Hospitalization102,610
Death22,817
Disabling15,123
Life-threatening11,609
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 28,692 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
10888-0140-01 You're viewing this 20000 CAPSULE, LIQUID FILLED in 1 CARTON (10888-0140-1) Active

🧭 About this NDC listing & data coverage

Bulk ingredient (not a finished retail product)

This is a bulk ingredient listing — not a retail prescription package

ERGOCALCIFEROL 1.25 mg/1 CAPSULE, LIQUID FILLED is listed with FDA as a bulk ingredient (a drug substance supplied for further manufacturing or licensed pharmacy compounding). It is not a finished product a patient would receive at a retail pharmacy, so consumer-style information — a patient label, retail pricing, package photos — generally does not exist for this NDC. The listing identifies the substance and package for supply-chain and regulatory purposes.

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 — 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 "Bulk Ingredient For Human Prescription Compounding". 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.
Can I get this product filled at a pharmacy?
Not as listed here. A bulk ingredient NDC identifies drug substance supplied for manufacturing or licensed compounding — it is not a finished, dispensable package. A pharmacy prescription would involve a finished product with its own NDC.
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 10888-0140-1, 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: 10888-0140-01, written without dashes as 10888014001. 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 10888-0140-01, the first segment (10888) is the labeler code FDA assigned to Banner Pharmacaps Inc.; the middle segment (0140) 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 Banner Pharmacaps Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Banner Pharmacaps 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.
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.

📄 Full FDA label FDA SPL

The complete FDA label for this product, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
📄 FDA label 19 words

No FDA label is on file for this product yet. Labels load from openFDA / DailyMed and refresh weekly.

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