methocarbamol

Generic: methocarbamol

Labeler: unichem pharmaceuticals (usa), inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methocarbamol
Generic Name methocarbamol
Labeler unichem pharmaceuticals (usa), inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

methocarbamol 500 mg/1

Manufacturer
UNICHEM PHARMACEUTICALS (USA), INC.

Identifiers & Regulatory

Product NDC 76385-123
Product ID 76385-123_1739d3e9-4645-4a0e-bec4-727f8ec63c23
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208507
Listing Expiration 2027-12-31
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 76385123
Hyphenated Format 76385-123

Supplemental Identifiers

RxCUI
197943 197944
UNII
125OD7737X
NUI
N0000175730 N0000175737

Packaging Origin

Original Packager
true

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
  • 500 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (76385-123-01)
  • 500 TABLET, FILM COATED in 1 BOTTLE (76385-123-50)
source: ndc

Packages (2)

76385-123-01 100 TABLET, FILM COATED in 1 BOTTLE (76385-123-01) 76385-123-50 500 TABLET, FILM COATED in 1 BOTTLE (76385-123-50)

Ingredients (1)

methocarbamol (500 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": "1739d3e9-4645-4a0e-bec4-727f8ec63c23", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197943", "197944"], "spl_set_id": ["5777cbb0-b5fd-4b36-ac1d-bc105fe96888"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["UNICHEM PHARMACEUTICALS (USA), INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (76385-123-01)", "package_ndc": "76385-123-01", "marketing_start_date": "20180115"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (76385-123-50)", "package_ndc": "76385-123-50", "marketing_start_date": "20180115"}], "brand_name": "Methocarbamol", "product_id": "76385-123_1739d3e9-4645-4a0e-bec4-727f8ec63c23", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "76385-123", "generic_name": "Methocarbamol", "labeler_name": "UNICHEM PHARMACEUTICALS (USA), INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "500 mg/1"}], "application_number": "ANDA208507", "marketing_category": "ANDA", "marketing_start_date": "20180115", "listing_expiration_date": "20271231"}