methocarbamol

Generic: methocarbamol

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methocarbamol
Generic Name methocarbamol
Labeler major pharmaceuticals
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methocarbamol 750 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-7058
Product ID 0904-7058_f24af140-d1ae-48a7-9d58-0a698f0aa0b4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA086988
Listing Expiration 2027-12-31
Marketing Start 2013-01-15

Pharmacologic Class

Established (EPC)
muscle relaxant [epc]
Physiologic Effect
centrally-mediated muscle relaxation [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09047058
Hyphenated Format 0904-7058

Supplemental Identifiers

RxCUI
197943 197944
UNII
125OD7737X
NUI
N0000175730 N0000175737

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name methocarbamol (source: ndc)
Generic Name methocarbamol (source: ndc)
Application Number ANDA086988 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (0904-7058-61) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

0904-7058-61 100 BLISTER PACK in 1 CARTON (0904-7058-61) / 1 TABLET in 1 BLISTER PACK

Ingredients (1)

methocarbamol (750 mg/1)

Linked Drug Pages (1)

Methocarbamol ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f24af140-d1ae-48a7-9d58-0a698f0aa0b4", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197943", "197944"], "spl_set_id": ["2df34fa7-9cdc-4be4-ac6f-577122462606"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7058-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7058-61", "marketing_start_date": "20130115"}], "brand_name": "Methocarbamol", "product_id": "0904-7058_f24af140-d1ae-48a7-9d58-0a698f0aa0b4", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "0904-7058", "generic_name": "Methocarbamol", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "750 mg/1"}], "application_number": "ANDA086988", "marketing_category": "ANDA", "marketing_start_date": "20130115", "listing_expiration_date": "20271231"}