methocarbamol

Generic: methocarbamol

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methocarbamol
Generic Name methocarbamol
Labeler nucare pharmaceuticals,inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

methocarbamol 750 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-3859
Product ID 68071-3859_485d986c-7678-9b95-e063-6394a90a43ea
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213967
Listing Expiration 2027-12-31
Marketing Start 2020-08-12

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 680713859
Hyphenated Format 68071-3859

Supplemental Identifiers

RxCUI
197944
UPC
0368071385922
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 ANDA213967 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 20 TABLET, FILM COATED in 1 BOTTLE (68071-3859-2)
  • 30 TABLET, FILM COATED in 1 BOTTLE (68071-3859-3)
  • 90 TABLET, FILM COATED in 1 BOTTLE (68071-3859-9)
source: ndc

Packages (3)

68071-3859-2 20 TABLET, FILM COATED in 1 BOTTLE (68071-3859-2) 68071-3859-3 30 TABLET, FILM COATED in 1 BOTTLE (68071-3859-3) 68071-3859-9 90 TABLET, FILM COATED in 1 BOTTLE (68071-3859-9)

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": "485d986c-7678-9b95-e063-6394a90a43ea", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0368071385922"], "unii": ["125OD7737X"], "rxcui": ["197944"], "spl_set_id": ["36c2c31c-8648-7723-e063-6294a90aec98"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68071-3859-2)", "package_ndc": "68071-3859-2", "marketing_start_date": "20250604"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-3859-3)", "package_ndc": "68071-3859-3", "marketing_start_date": "20251224"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68071-3859-9)", "package_ndc": "68071-3859-9", "marketing_start_date": "20250114"}], "brand_name": "Methocarbamol", "product_id": "68071-3859_485d986c-7678-9b95-e063-6394a90a43ea", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "68071-3859", "generic_name": "Methocarbamol", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "750 mg/1"}], "application_number": "ANDA213967", "marketing_category": "ANDA", "marketing_start_date": "20200812", "listing_expiration_date": "20271231"}