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United States · US · US:71335-2383_df5480a3-34e1-49de-9178-9fb5d8368516

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
    7133523830
    15 TABLET in 1 BOTTLE (71335-2383-0)
  • ndc11
    7133523831
    14 TABLET in 1 BOTTLE (71335-2383-1)
  • ndc11
    7133523832
    30 TABLET in 1 BOTTLE (71335-2383-2)
  • ndc11
    7133523833
    20 TABLET in 1 BOTTLE (71335-2383-3)
  • ndc11
    7133523834
    60 TABLET in 1 BOTTLE (71335-2383-4)
  • ndc11
    7133523835
    100 TABLET in 1 BOTTLE (71335-2383-5)
  • ndc11
    7133523836
    40 TABLET in 1 BOTTLE (71335-2383-6)
  • ndc11
    7133523837
    90 TABLET in 1 BOTTLE (71335-2383-7)
  • ndc11
    7133523838
    120 TABLET in 1 BOTTLE (71335-2383-8)
  • ndc11
    7133523839
    7 TABLET in 1 BOTTLE (71335-2383-9)

Annotations

UNII (FDA Substance ID)
125OD7737X
METHOCARBAMOL
RxCUI 6845
Orange Book
A040489
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": "71335-2383_df5480a3-34e1-49de-9178-9fb5d8368516",
  "productndc": "71335-2383",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "040489",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AA",
        "strength": "500MG",
        "product_no": "001",
        "approval_date": "Jan 29, 2003"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AA",
        "strength": "750MG",
        "product_no": "002",
        "approval_date": "Jan 29, 2003"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "METHOCARBAMOL",
  "proprietary_name": "Methocarbamol",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA040489",
  "marketing_category": "ANDA",
  "nonproprietary_name": "methocarbamol",
  "start_marketing_date": "20190815",
  "active_numerator_strength": "500"
}

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