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Methocarbamol - 68387-340-90 - (Methocarbamol)

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Drug Information of Methocarbamol

Product NDC: 68387-340
Proprietary Name: Methocarbamol
Non Proprietary Name: Methocarbamol
Active Ingredient(s): 750    mg/1 & nbsp;   Methocarbamol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Methocarbamol

Product NDC: 68387-340
Labeler Name: Keltman Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA085159
Marketing Category: ANDA
Start Marketing Date: 20070725

Package Information of Methocarbamol

Package NDC: 68387-340-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (68387-340-90)

NDC Information of Methocarbamol

NDC Code 68387-340-90
Proprietary Name Methocarbamol
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (68387-340-90)
Product NDC 68387-340
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methocarbamol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070725
Marketing Category Name ANDA
Labeler Name Keltman Pharmaceuticals Inc.
Substance Name METHOCARBAMOL
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

Complete Information of Methocarbamol


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