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United States · US · US:76420-894_2cbe9e1b-d4dc-de70-e063-6394a90a18b8

Methocarbamol

Orange BookUNIISPLATC M03BA53

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerAsclemed USA, Inc.
CountryUS (United States)
ATC codeM03BA53
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 6

  • ndc11
    7642089401
    100 TABLET, COATED in 1 BOTTLE (76420-894-01)
  • ndc11
    7642089405
    500 TABLET, COATED in 1 BOTTLE (76420-894-05)
  • ndc11
    7642089412
    120 TABLET, COATED in 1 BOTTLE (76420-894-12)
  • ndc11
    7642089430
    30 TABLET, COATED in 1 BOTTLE (76420-894-30)
  • ndc11
    7642089460
    60 TABLET, COATED in 1 BOTTLE (76420-894-60)
  • ndc11
    7642089490
    90 TABLET, COATED in 1 BOTTLE (76420-894-90)

Annotations

UNII (FDA Substance ID)
125OD7737X
METHOCARBAMOL
RxCUI 6845
Orange Book
A209312
AAAA
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "125OD7737X",
    "rxcui": "6845",
    "inchikey": "GNXFOGHNGIVQEH-UHFFFAOYSA-N",
    "display_name": "METHOCARBAMOL",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "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": "76420-894_2cbe9e1b-d4dc-de70-e063-6394a90a18b8",
  "productndc": "76420-894",
  "dosage_form": "TABLET, COATED",
  "orange_book": {
    "appl_no": "209312",
    "products": [
      {
        "rs": true,
        "rld": false,
        "te_code": "AA",
        "strength": "500MG",
        "product_no": "001",
        "approval_date": "May 7, 2018"
      },
      {
        "rs": true,
        "rld": false,
        "te_code": "AA",
        "strength": "750MG",
        "product_no": "002",
        "approval_date": "May 7, 2018"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "METHOCARBAMOL",
  "proprietary_name": "Methocarbamol",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA209312",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Methocarbamol Tablets",
  "start_marketing_date": "20180702",
  "active_numerator_strength": "750"
}

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