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
Routes
ORAL
Active Ingredients

methocarbamol 750 mg/1

Manufacturer
Aphena Pharma Solutions - Tennessee, LLC

Identifiers & Regulatory

Product NDC 71610-598
Product ID 71610-598_0d749d2c-80a9-4bc4-975e-cd9475de438a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA086988
Listing Expiration 2026-12-31
Marketing Start 1982-01-01

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 71610598
Hyphenated Format 71610-598

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
  • 60 TABLET in 1 BOTTLE (71610-598-53)
  • 90 TABLET in 1 BOTTLE (71610-598-60)
  • 120 TABLET in 1 BOTTLE (71610-598-70)
  • 180 TABLET in 1 BOTTLE (71610-598-80)
source: ndc

Packages (4)

Ingredients (1)

methocarbamol (750 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0d749d2c-80a9-4bc4-975e-cd9475de438a", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197943", "197944"], "spl_set_id": ["27c39343-44e0-4ca6-a67f-1e6d11dd6799"], "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 in 1 BOTTLE (71610-598-53)", "package_ndc": "71610-598-53", "marketing_start_date": "20210909"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71610-598-60)", "package_ndc": "71610-598-60", "marketing_start_date": "20210909"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71610-598-70)", "package_ndc": "71610-598-70", "marketing_start_date": "20210909"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71610-598-80)", "package_ndc": "71610-598-80", "marketing_start_date": "20210909"}], "brand_name": "Methocarbamol", "product_id": "71610-598_0d749d2c-80a9-4bc4-975e-cd9475de438a", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "71610-598", "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": "ANDA086988", "marketing_category": "ANDA", "marketing_start_date": "19820101", "listing_expiration_date": "20261231"}