methocarbamol

Generic: methocarbamol

Labeler: aphena pharma solutions - tennessee, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methocarbamol
Generic Name methocarbamol
Labeler aphena pharma solutions - tennessee, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

methocarbamol 750 mg/1

Manufacturer
Aphena Pharma Solutions - Tennessee, LLC

Identifiers & Regulatory

Product NDC 71610-174
Product ID 71610-174_0cd04c66-6852-4320-add6-5272c3f92dc9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208507
Listing Expiration 2026-12-31
Marketing Start 2018-01-15

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 71610174
Hyphenated Format 71610-174

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 (source: ndc)
Application Number ANDA208507 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 60 TABLET, FILM COATED in 1 BOTTLE (71610-174-53)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71610-174-60)
  • 120 TABLET, FILM COATED in 1 BOTTLE (71610-174-70)
  • 180 TABLET, FILM COATED in 1 BOTTLE (71610-174-80)
source: ndc

Packages (4)

71610-174-53 60 TABLET, FILM COATED in 1 BOTTLE (71610-174-53) 71610-174-60 90 TABLET, FILM COATED in 1 BOTTLE (71610-174-60) 71610-174-70 120 TABLET, FILM COATED in 1 BOTTLE (71610-174-70) 71610-174-80 180 TABLET, FILM COATED in 1 BOTTLE (71610-174-80)

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": "0cd04c66-6852-4320-add6-5272c3f92dc9", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197944"], "spl_set_id": ["d825e4d6-8b00-473a-a6e6-90f5c3ad5bec"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71610-174-53)", "package_ndc": "71610-174-53", "marketing_start_date": "20181022"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71610-174-60)", "package_ndc": "71610-174-60", "marketing_start_date": "20181022"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71610-174-70)", "package_ndc": "71610-174-70", "marketing_start_date": "20181022"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (71610-174-80)", "package_ndc": "71610-174-80", "marketing_start_date": "20181022"}], "brand_name": "Methocarbamol", "product_id": "71610-174_0cd04c66-6852-4320-add6-5272c3f92dc9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "71610-174", "generic_name": "Methocarbamol", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "750 mg/1"}], "application_number": "ANDA208507", "marketing_category": "ANDA", "marketing_start_date": "20180115", "listing_expiration_date": "20261231"}