United States· US:60687-568_22058b66-8c4a-4a0b-e063-6394a90ae73e
Methocarbamol
A methocarbamol, kombinationen, exkl. psycholeptika product containing methocarbamol, registered in United States by American Health Packaging. The same ATC class is registered in 4 of our 19 countries.
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
Where it is registered
Methocarbamol, kombinationen, exkl. psycholeptika is registered in 4 of 19 countries.
Countries holding a registration under ATC M03BA53 (methocarbamol, kombinationen, exkl. psycholeptika), each read from that country’s own register.
- This record: United States, from FDA National Drug Code directory (United States)
- 3 of them publish a price we can compare per daily dose
Methocarbamol, kombinationen, exkl. psycholeptika · ATC M03BA53
4 / 19 countries
- Canada
- Finlandprice
- Polandprice
- United Statesprice
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- Methocarbamol
- Manufacturer
- American Health Packaging
- Country
- United States (US)
- ATC code
- M03BA53
- ATC class
- Methocarbamol, Kombinationen, exkl. Psycholeptika
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- September 12, 2026
Packs & prices · 1
- ndc116068756801100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-568-01) / 1 TABLET in 1 BLISTER PACK (60687-568-11)
Regulatory notes
Same medicine, other countries
Methocarbamol, kombinationen, exkl. psycholeptika in 11 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United KingdomMethocarbamol 750mg tabletsAccord-UK Ltd
- SwitzerlandMetoflex 750 mg, comprimésLabatec Pharma SA
- CanadaROBAXIN 750HALEON CANADA ULC
- FinlandRobaxinJohn Wyeth & Brother Ltd
- NorwayOrtotonRecordati
- GermanyMethocaPuren Pharma Gmbh & Co. Kg
- CzechiaDOLIROBAXGOODWILL PHARMA Plc., Szeged
- SpainDOLIROBAX 500 MG COMPRIMIDOSFaes Farma S.A.
Authorised across Europe · EMA
The same active substance is authorised in 12 EEA countries. Names it is sold under:
- Austria · Methocarbamol Kwizda
- Czechia · Dolirobax
- Germany · Methoca, Methocarbamol Al
- Spain · Dolirobax, Molitrem
- France · Lumirelax, Methocarbamol Arrow
- United Kingdom (Northern Ireland) · Methocarbamol Activase Pharmaceuticals, Methocarbamol Amarox
- Hungary · Dolirobax Tabletta
- Luxembourg · Methocarbamol Micro Labs
- Malta · Rolaxifor
- Poland · Methocarbamol Espefa
- Portugal · Robaxisal, Zelaz
- Slovakia · Dolirobax
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/4fac09f1-76fd-4f38-b68a-b13b9e964222 GET /v1/drugs/4fac09f1-76fd-4f38-b68a-b13b9e964222?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": "125OD7737X",
"rxcui": "6845",
"inchikey": "GNXFOGHNGIVQEH-UHFFFAOYSA-N",
"display_name": "METHOCARBAMOL",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"livertox": {
"summary": null,
"livertox_id": null,
"hepatotoxicity_score": 5
},
"spl_meta": {
"3212f121-9428-4186-8f00-accf08bca473": {
"match": "brand_token",
"title": "METHOCARBAMOL TABLET, FILM COATED [BRYANT RANCH PREPACK]",
"spl_version": "7",
"published_date": "2026-06-01"
}
},
"productid": "60687-568_22058b66-8c4a-4a0b-e063-6394a90ae73e",
"productndc": "60687-568",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "090200",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AA",
"strength": "500MG",
"product_no": "001",
"approval_date": "Nov 6, 2009"
},
{
"rs": false,
"rld": false,
"te_code": "AA",
"strength": "750MG",
"product_no": "002",
"approval_date": "Nov 6, 2009"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "METHOCARBAMOL",
"proprietary_name": "Methocarbamol",
"active_ingred_unit": "mg/1",
"application_number": "ANDA090200",
"marketing_category": "ANDA",
"nonproprietary_name": "Methocarbamol",
"start_marketing_date": "20200520",
"active_numerator_strength": "750"
}See everything about methocarbamol, kombinationen, exkl. psycholeptika.
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.