methocarbamol

Generic: methocarbamol tablets

Labeler: denton pharma, inc. dba northwind pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methocarbamol
Generic Name methocarbamol tablets
Labeler denton pharma, inc. dba northwind pharmaceuticals
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

methocarbamol 750 mg/1

Manufacturer
Denton Pharma, Inc. dba Northwind Pharmaceuticals

Identifiers & Regulatory

Product NDC 70934-756
Product ID 70934-756_de1d004b-f814-03a5-e053-2a95a90a2b58
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209312
Marketing Start 2020-05-29
Marketing End 2026-03-31

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 70934756
Hyphenated Format 70934-756

Supplemental Identifiers

RxCUI
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 tablets (source: ndc)
Application Number ANDA209312 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 30 TABLET, COATED in 1 BOTTLE, PLASTIC (70934-756-30)
source: ndc

Packages (1)

70934-756-30 30 TABLET, COATED in 1 BOTTLE, PLASTIC (70934-756-30)

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": "de1d004b-f814-03a5-e053-2a95a90a2b58", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197944"], "spl_set_id": ["a9c763e1-1b3e-3b4c-e053-2a95a90a9404"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Denton Pharma, Inc. dba Northwind Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE, PLASTIC (70934-756-30)", "package_ndc": "70934-756-30", "marketing_end_date": "20260331", "marketing_start_date": "20220503"}], "brand_name": "Methocarbamol", "product_id": "70934-756_de1d004b-f814-03a5-e053-2a95a90a2b58", "dosage_form": "TABLET, COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "70934-756", "generic_name": "Methocarbamol Tablets", "labeler_name": "Denton Pharma, Inc. dba Northwind Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "750 mg/1"}], "application_number": "ANDA209312", "marketing_category": "ANDA", "marketing_end_date": "20260331", "marketing_start_date": "20200529"}