NDC 68788-9076

Methocarbamol

Methocarbamol

Methocarbamol is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Preferred Pharmaceuticals, Inc.. The primary component is Methocarbamol.

Product ID68788-9076_d811c4cd-7f31-419c-bc75-7414007f8ac1
NDC68788-9076
Product TypeHuman Prescription Drug
Proprietary NameMethocarbamol
Generic NameMethocarbamol
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2010-08-06
Marketing CategoryANDA / ANDA
Application NumberANDA040489
Labeler NamePreferred Pharmaceuticals, Inc.
Substance NameMETHOCARBAMOL
Active Ingredient Strength750 mg/1
Pharm ClassesCentrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 68788-9076-1

100 TABLET in 1 BOTTLE, DISPENSING (68788-9076-1)
Marketing Start Date2010-08-06
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68788-9076-3 [68788907603]

Methocarbamol TABLET
Marketing CategoryANDA
Application NumberANDA040489
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-08-06
Marketing End Date2019-10-28

NDC 68788-9076-1 [68788907601]

Methocarbamol TABLET
Marketing CategoryANDA
Application NumberANDA040489
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-08-06
Marketing End Date2019-10-28

NDC 68788-9076-9 [68788907609]

Methocarbamol TABLET
Marketing CategoryANDA
Application NumberANDA040489
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-08-06
Marketing End Date2019-10-28

NDC 68788-9076-4 [68788907604]

Methocarbamol TABLET
Marketing CategoryANDA
Application NumberANDA040489
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-08-06
Marketing End Date2019-10-28

NDC 68788-9076-6 [68788907606]

Methocarbamol TABLET
Marketing CategoryANDA
Application NumberANDA040489
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-08-06
Marketing End Date2019-10-28

NDC 68788-9076-8 [68788907608]

Methocarbamol TABLET
Marketing CategoryANDA
Application NumberANDA040489
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-08-06
Marketing End Date2019-10-28

NDC 68788-9076-2 [68788907602]

Methocarbamol TABLET
Marketing CategoryANDA
Application NumberANDA040489
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-08-06
Marketing End Date2019-10-28

Drug Details

Active Ingredients

IngredientStrength
METHOCARBAMOL750 mg/1

OpenFDA Data

SPL SET ID:8a6ab350-2e0a-4809-b943-8bd1e7b0f779
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197943
  • 197944

    • Pharmacological Class

    • Centrally-mediated Muscle Relaxation [PE]
    • Muscle Relaxant [EPC]

    NDC Crossover Matching brand name "Methocarbamol" or generic name "Methocarbamol"

    NDCBrand NameGeneric Name
    0143-1290MethocarbamolMethocarbamol
    0143-1292MethocarbamolMethocarbamol
    0179-0092MethocarbamolMethocarbamol
    0276-0510MethocarbamolMethocarbamol
    0404-9909MethocarbamolMethocarbamol
    0440-1740Methocarbamolmethocarbamol
    0517-1825Methocarbamolmethocarbamol
    0603-4485Methocarbamolmethocarbamol
    0603-4486Methocarbamolmethocarbamol
    0615-7572Methocarbamolmethocarbamol
    0615-7573Methocarbamolmethocarbamol
    0615-8435METHOCARBAMOLMETHOCARBAMOL
    0615-8436METHOCARBAMOLMETHOCARBAMOL
    0904-7057MethocarbamolMethocarbamol
    0904-7058MethocarbamolMethocarbamol
    10135-664MethocarbamolMethocarbamol
    10135-665MethocarbamolMethocarbamol
    10544-259MethocarbamolMethocarbamol
    10544-464MethocarbamolMethocarbamol
    10544-622MethocarbamolMethocarbamol
    10544-773MethocarbamolMethocarbamol
    10544-956Methocarbamolmethocarbamol
    17511-505METHOCARBAMOLMETHOCARBAMOL
    17511-506METHOCARBAMOLMETHOCARBAMOL
    21695-078MethocarbamolMethocarbamol
    21695-079MethocarbamolMethocarbamol
    68071-1874MethocarbamolMethocarbamol
    68071-4365MethocarbamolMethocarbamol
    68071-4458MethocarbamolMethocarbamol
    68071-4505MethocarbamolMethocarbamol
    68083-317MethocarbamolMethocarbamol
    68084-056MethocarbamolMethocarbamol
    68071-4520MethocarbamolMethocarbamol
    68084-057MethocarbamolMethocarbamol
    68151-2775MethocarbamolMethocarbamol
    68387-340MethocarbamolMethocarbamol
    68387-342MethocarbamolMethocarbamol
    68475-002MethocarbamolMethocarbamol
    68788-6391MethocarbamolMethocarbamol
    68788-9076MethocarbamolMethocarbamol
    68788-9075MethocarbamolMethocarbamol
    68788-9388MethocarbamolMethocarbamol
    68788-9768MethocarbamolMethocarbamol
    68788-9376MethocarbamolMethocarbamol
    69543-134MethocarbamolMethocarbamol
    69543-135MethocarbamolMethocarbamol
    70010-754MethocarbamolMethocarbamol
    70069-101MethocarbamolMethocarbamol
    70010-770MethocarbamolMethocarbamol
    70518-0024MethocarbamolMethocarbamol
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