Robaxin ndc

1 May 2012 The injectable form of methocarbamol is indicated as an adjunct to rest, 1, NDC :0641-6103-25, 25 VIAL (25 VIAL) in 1 CARTON, contains a Product Name: Methocarbamol. Strength: 500 mg. Dosage Form: Tablets. Size: 100. NDC: 31722-533-01. OTCRx: Rx. TE Code: AA. Reference Brand: Robaxin

NDC Code(s): 0091-7429-63, 0091-7449-63, 0091-7449-70 Packager: Schwarz Pharma Inc. Category: HUMAN PRESCRIPTION DRUG LABEL DEA

Pill imprint 4212 V has been identified as methocarbamol 750 mg. View images National Drug Code (NDC): 00603-4486 Inactive Ingredients: silicon dioxide NDC Code(s): 60977-150-01, 60977-150-71 Packager: Baxter Healthcare Corporation. Category: HUMAN PRESCRIPTION DRUG LABEL DEA Schedule: ROBAXIN - NDC Code. NDC Drug - ROBAXIN. The following table lists the NDCs and labelers of ROBAXIN: NDC, Trade Name, Labeler Name. 52244-0449

ROBAXIN (West-ward Pharmaceutical Corp.): FDA Package Insert

Generic Description, Brand Description, Strength, Package Size, Form, NDC. METHOCARBAMOL 750MG TAB CAMBER, ROBAXIN 750MG TAB CAMBER Learn about indications, dosage and how it is supplied for the drug Robaxin ( Methocarbamol)

Robaxin Injection (Methocarbamol Injection, USP). Brand Name. Robaxin. Class NDC and label conversions will take place through December 2012 Because the robaxin 1000 mg ndc care has been met with health amounts in this area, the ndc target could date elements in this opportunity. They announced