United States· US:51662-1235_103601ca-3a98-74c4-e063-6294a90a524c
50% MAGNESIUM SULFATE
A magnesium sulfate product containing 50% magnesium sulfate, registered in United States by HF Acquisition Co. LLC, DBA Health First. The same ATC class is registered in 2 of our 19 countries.
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
Where it is registered
Magnesium sulfate is registered in 2 of 19 countries.
Countries holding a registration under ATC D11AX05 (magnesium sulfate), each read from that country’s own register.
- This record: United States, from FDA National Drug Code directory (United States)
- 1 of them publish a price we can compare per daily dose
Magnesium sulfate · ATC D11AX05
2 / 19 countries
- Ireland
- United Statesprice
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- 50% MAGNESIUM SULFATE
- Manufacturer
- HF Acquisition Co. LLC, DBA Health First
- Country
- United States (US)
- ATC code
- D11AX05
- ATC class
- Magnesium sulfate
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- June 3, 2026
Packs & prices · 2
- ndc1151662123511 SYRINGE, PLASTIC in 1 CARTON (51662-1235-1) / 10 mL in 1 SYRINGE, PLASTIC
- ndc11516621235310 POUCH in 1 CASE (51662-1235-3) / 1 CARTON in 1 POUCH (51662-1235-2) / 1 SYRINGE, PLASTIC in 1 CARTON / 10 mL in 1 SYRINGE, PLASTIC
Regulatory notes
Same medicine, other countries
Magnesium sulfate in 11 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United KingdomAquaDerm Hydrous ointmentImpectron Ltd
- FranceSPASMAG INJECTABLE, solution injectable (IV) en ampouleGRIMBERG
- NetherlandsMagnesiumsulfaat Eureco-Pharma 100 mg/ml, oplossing voor injectieEureco-Pharma B.V.
- CanadaMAGNESIUM SULFATE IN WATER FOR INJECTIONBAXTER CORPORATION
- PolandInj. Magnesii Sulfurici 20% PolpharmaZakłady Farmaceutyczne POLPHARMA S.A.
- SpainSULFATO DE MAGNESIO ALTAN 150 MG/ML SOLUCION INYECTABLE Y PARA PERFUSION EFGAltan Pharmaceuticals Sa
- FinlandAddex-MagnesiumsulfaattiFresenius Kabi AB
- Japan硫酸マグネシウム水和物
Authorised across Europe · EMA
The same active substance is authorised in 6 EEA countries. Names it is sold under:
- Denmark · Magnesiumsulfat Sad
- France · Sulfate De Magnesium Renaudin
- United Kingdom (Northern Ireland) · Magnesium Sulphate Phoenix Labs
- Greece · Magnesium Sulfate Ariti
- Ireland · Magnesium Sulfate Foran Healthcare
- Netherlands · Magnesiiumsulfaat Teva, Magnesiumsulfaat Teva
Source: European Medicines Agency, Article 57 product data.
Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of FDA National Drug Code directory (United States). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.
For developers
The same record over the API, and the raw payload
GET /v1/drugs/ef3cd87b-51dd-4370-a756-d7bb7312c56f GET /v1/drugs/ef3cd87b-51dd-4370-a756-d7bb7312c56f?format=fhir
Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.
{
"unii": {
"unii": "SK47B8698T",
"rxcui": "236741",
"inchikey": "WRUGWIBCXHJTDG-UHFFFAOYSA-L",
"display_name": "MAGNESIUM SULFATE HEPTAHYDRATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAMUSCULAR; INTRAVENOUS",
"spl_meta": {
"698bede7-4fc1-4e85-8ac4-d735f409cfae": {
"match": "brand_token",
"title": "50% RUBBING (ISOPROPYL ALCOHOL) LIQUID [PERRIGO DIRECT, INC]",
"spl_version": "15",
"published_date": "2026-04-08"
}
},
"productid": "51662-1235_103601ca-3a98-74c4-e063-6294a90a524c",
"productndc": "51662-1235",
"dosage_form": "INJECTION, SOLUTION",
"orange_book": {
"appl_no": "075151",
"products": [
{
"rs": true,
"rld": false,
"te_code": "AP",
"strength": "5GM/10ML (500MG/ML)",
"product_no": "001",
"approval_date": "Apr 25, 2000"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "MAGNESIUM SULFATE HEPTAHYDRATE",
"proprietary_name": "50% MAGNESIUM SULFATE",
"active_ingred_unit": "mg/mL",
"application_number": "ANDA075151",
"marketing_category": "ANDA",
"nonproprietary_name": "50% MAGNESIUM SULFATE",
"start_marketing_date": "20180825",
"active_numerator_strength": "500"
}See everything about magnesium sulfate.
This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.