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United States · US · US:71335-0970_7736f8d3-1fbe-4989-8668-238b52974a54

Methocarbamol

Orange BookUNIISPLATC M03BA53

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

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeM03BA53
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 10

  • ndc11
    7133509700
    15 TABLET, FILM COATED in 1 BOTTLE (71335-0970-0)
  • ndc11
    7133509701
    14 TABLET, FILM COATED in 1 BOTTLE (71335-0970-1)
  • ndc11
    7133509702
    30 TABLET, FILM COATED in 1 BOTTLE (71335-0970-2)
  • ndc11
    7133509703
    20 TABLET, FILM COATED in 1 BOTTLE (71335-0970-3)
  • ndc11
    7133509704
    60 TABLET, FILM COATED in 1 BOTTLE (71335-0970-4)
  • ndc11
    7133509705
    100 TABLET, FILM COATED in 1 BOTTLE (71335-0970-5)
  • ndc11
    7133509706
    40 TABLET, FILM COATED in 1 BOTTLE (71335-0970-6)
  • ndc11
    7133509707
    90 TABLET, FILM COATED in 1 BOTTLE (71335-0970-7)
  • ndc11
    7133509708
    120 TABLET, FILM COATED in 1 BOTTLE (71335-0970-8)
  • ndc11
    7133509709
    7 TABLET, FILM COATED in 1 BOTTLE (71335-0970-9)

Annotations

UNII (FDA Substance ID)
125OD7737X
METHOCARBAMOL
RxCUI 6845
Orange Book
A208507
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": "71335-0970_7736f8d3-1fbe-4989-8668-238b52974a54",
  "productndc": "71335-0970",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "208507",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AA",
        "strength": "500MG",
        "product_no": "001",
        "approval_date": "Jul 21, 2017"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AA",
        "strength": "750MG",
        "product_no": "002",
        "approval_date": "Jul 21, 2017"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "METHOCARBAMOL",
  "proprietary_name": "Methocarbamol",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA208507",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Methocarbamol",
  "start_marketing_date": "20180115",
  "active_numerator_strength": "500"
}

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