methocarbamol

Generic: methocarbamol tablets

Labeler: phoenix rx llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methocarbamol
Generic Name methocarbamol tablets
Labeler phoenix rx llc
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

methocarbamol 750 mg/1

Manufacturer
PHOENIX RX LLC

Identifiers & Regulatory

Product NDC 85509-1770
Product ID 85509-1770_414b513b-bb1e-014d-e063-6294a90a7a90
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209312
Listing Expiration 2026-12-31
Marketing Start 2018-07-02

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 855091770
Hyphenated Format 85509-1770

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 (85509-1770-3)
  • 60 TABLET, COATED in 1 BOTTLE (85509-1770-6)
  • 90 TABLET, COATED in 1 BOTTLE (85509-1770-9)
source: ndc

Packages (3)

85509-1770-3 30 TABLET, COATED in 1 BOTTLE (85509-1770-3) 85509-1770-6 60 TABLET, COATED in 1 BOTTLE (85509-1770-6) 85509-1770-9 90 TABLET, COATED in 1 BOTTLE (85509-1770-9)

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": "414b513b-bb1e-014d-e063-6294a90a7a90", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197944"], "spl_set_id": ["414b2fe0-fa2b-2b18-e063-6394a90ab2b9"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["PHOENIX RX LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (85509-1770-3)", "package_ndc": "85509-1770-3", "marketing_start_date": "20251016"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (85509-1770-6)", "package_ndc": "85509-1770-6", "marketing_start_date": "20251016"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (85509-1770-9)", "package_ndc": "85509-1770-9", "marketing_start_date": "20251016"}], "brand_name": "Methocarbamol", "product_id": "85509-1770_414b513b-bb1e-014d-e063-6294a90a7a90", "dosage_form": "TABLET, COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "85509-1770", "generic_name": "Methocarbamol Tablets", "labeler_name": "PHOENIX RX LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "750 mg/1"}], "application_number": "ANDA209312", "marketing_category": "ANDA", "marketing_start_date": "20180702", "listing_expiration_date": "20261231"}