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NDC 61919-0616-60 Methocarbamol 750 mg/1 Details
Methocarbamol 750 mg/1
Methocarbamol is a ORAL TABLET, COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by DIRECT RX. The primary component is METHOCARBAMOL.
MedlinePlus Drug Summary
Methocarbamol is used with rest, physical therapy, and other measures to relax muscles and relieve pain and discomfort caused by strains, sprains, and other muscle injuries. Methocarbamol is in a class of medications called muscle relaxants. It works by slowing activity in the nervous system to allow the body to relax
Related Packages: 61919-0616-60Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Methocarbamol
Product Information
NDC | 61919-0616 |
---|---|
Product ID | 61919-616_f9a195e8-e094-672b-e053-6394a90a94e6 |
Associated GPIs | 75100070000310 |
GCN Sequence Number | 004655 |
GCN Sequence Number Description | methocarbamol TABLET 750 MG ORAL |
HIC3 | H6H |
HIC3 Description | SKELETAL MUSCLE RELAXANTS |
GCN | 17893 |
HICL Sequence Number | 001938 |
HICL Sequence Number Description | METHOCARBAMOL |
Brand/Generic | Generic |
Proprietary Name | Methocarbamol |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Methocarbamol |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | TABLET, COATED |
Route | ORAL |
Active Ingredient Strength | 750 |
Active Ingredient Units | mg/1 |
Substance Name | METHOCARBAMOL |
Labeler Name | DIRECT RX |
Pharmaceutical Class | Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA209312 |
Listing Certified Through | 2024-12-31 |
Package
NDC 61919-0616-60 (61919061660)
NDC Package Code | 61919-616-60 |
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Billing NDC | 61919061660 |
Package | 60 TABLET, COATED in 1 BOTTLE (61919-616-60) |
Marketing Start Date | 2019-04-18 |
NDC Exclude Flag | N |
Pricing Information | N/A |