![Angina Drops 2083 2 [hp_X]/59mL; 3 [hp_X]/59mL; 3 [hp_X]/59mL; 5 [hp_X]/59mL; 6 [hp_X]/59mL; 6 [hp_X]/59mL; 6 [hp_X]/59mL Liquid, 59 mL — NDC 63083-2083-02 package photo](https://dailymed.nlm.nih.gov/dailymed/image.cfm?setid=99516597-9f59-4123-bd35-a4a73dd54d2d&name=c83-thumb.jpg)
Angina Drops 2083 2 [hp_X]/59mL; 3 [hp_X]/59mL; 3 [hp_X]/59mL; 5 [hp_X]/59mL; 6 [hp_X]/59mL; 6 [hp_X]/59mL; 6 [hp_X]/59mL Liquid, 59 mL
by Professional Complementary Health Formulas · 59 mL in 1 BOTTLE, DROPPER (63083-2083-2)
NDC 63083-2083-02
🏷️ FDA NDC (as labeled)
63083-2083-2
billing pads the package segment with a zero
OTC
On market
Non-controlled
🗂️ Data synced Sep 17, 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)
63083-2083-2
Product NDC
63083-2083
11-digit billing NDC
63083208302
UNII
6OM09RPY36, 7114SV0MYK, 79N6542N18, 27YLU75U4W, S7V92P67HO, F1T8QT9U8B +6 more
SPL Set ID
99516597-9f59-4123-bd35-a4a73dd54d2d
Established class (EPC)
Nitrate Vasodilator
Physiologic effect
Vasodilation
Chemical class
Nitrates
DEA schedule
Non-controlled
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
1984-08-15
Route
ORAL
Dosage form
LIQUID
Substance
HAWTHORN LEAF WITH FLOWER; SELENICEREUS GRANDIFLORUS STEM; KALMIA LATIFOLIA LEAF; PHOSPHORUS; ARSENIC TRIOXIDE; DIGITALIS; NITROGLYCERIN; DRIMIA MARITIMA BULB; GELSEMIUM SEMPERVIRENS ROOT; SPIGELIA MARILANDICA ROOT; POTASSIUM CARBONATE; ARNICA MONTANA WHO
Why two NDCs?
The FDA registers this code as 63083-2083-2 — 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 → 63083-2083-02. 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
LabelerProfessional Complementary Health Formulas
Labeler code63083
First marketedAug 1984
Product typeHuman Otc Drug
Portfolio605 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.
🩺 Clinical
🧪 What is this product?
Angina Drops 2083 is a liquid oral homeopathic product containing multiple plant-derived and mineral substances traditionally used in homeopathic practice. The formulation includes ingredients such as arnica, gelsemium, hawthorn, and spigelia, which appear in homeopathic preparations typically used to address various conditions, along with nitroglycerin, digitalis, and arsenic trioxide. Homeopathic products are marketed based on traditional use rather than FDA evaluation for effectiveness. This product is not approved by the FDA and should not be relied upon as a substitute for conventional medical care.
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.
💬 Questions about Angina Drops?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
🧪 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 system | Per mL | 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.
🔁 Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Angina Drops 2083 2 [hp_X]/59mL; 3 [hp_X]/59mL; 3 [hp_X]/59mL; 5 [hp_X]/59mL; 6 [hp_X]/59mL; 6 [hp_X]/59mL; 6 [hp_X]/59mLthis 63083-2083-02 | Professional | 59 ml | — | — | 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
🏛️
1984
On the market since
Aug 1984
📍
2026
Currently FDA-listed
42 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.
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 63083-2083-02 You're viewing this | 59 mL in 1 BOTTLE, DROPPER (63083-2083-2) | 1985-08-15 | Active |
🧭 About this NDC listing & data coverage
Over-the-counter (OTC) product
Homeopathic listing
About homeopathic listings
Angina Drops 2083 2 [hp_X]/59mL; 3 [hp_X]/59mL; 3 [hp_X]/59mL; 5 [hp_X]/59mL; 6 [hp_X]/59mL; 6 [hp_X]/59mL; 6 [hp_X]/59mL LIQUID is listed under the homeopathic marketing category. An NDC listing in this category does not by itself establish FDA approval, and FDA does not evaluate homeopathic products for effectiveness. This page reports the listing data as published.
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) | — 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 "Unapproved Homeopathic". 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 63083-2083-2, 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: 63083-2083-02, written without dashes as 63083208302. 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 63083-2083-02, the first segment (63083) is the labeler code FDA assigned to Professional Complementary Health Formulas; the middle segment (2083) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (02) 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 Professional Complementary Health Formulas. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Professional Complementary Health Formulas 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.
📄 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
🎯 Indications and Usage ▾
INDICATIONS For the temporary relief of muscle cramps or spasms, muscular debility, mild abdominal, back or chest pain, or anxiousness.*
⏱️ Dosage and Administration ▾
DIRECTIONS Place drops under tongue 30 minutes before/after meals. Adults and children 12 years and over: Take 10 drops up to 3 times per day. Consult a physician for use in children under 12 years of age.
⚠️ Warnings ▾
WARNINGS Seek medical attention immediately for severe symptoms such as chest pressure or tightness with radiation of the pain to the jaw and down the arm, shortness of breath, or sweating. Keep out of the reach of children. In case of overdose, get medical help or contact a poison control center right away.
If pregnant or breastfeeding, ask a healthcare professional before use. Keep out of the reach of children. If pregnant or breastfeeding, ask a healthcare professional before use.
🧪 Active Ingredient ▾
ACTIVE INGREDIENTS Crataegus oxyacantha 2X Cactus grandiflorus 3X Kalmia latifolia 3X Phosphorus 5X Arsenicum album 6X Digitalis purpurea 6X Glonoinum 6X Scilla maritima 6X Gelsemium sempervirens 6X, 12X Spigelia marilandica 6X, 12X Kali carbonicum 12X, 30X Arnica montana 30X
🧪 Inactive Ingredients ▾
INACTIVE INGREDIENTS 20% ethanol, purified water.
🎯 Purpose ▾
*Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
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 ↗
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.