methocarbamol

Generic: methocarbamol

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

Drug Facts

Product Profile

Brand Name methocarbamol
Generic Name methocarbamol
Labeler preferred pharmaceuticals, inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methocarbamol 500 mg/1

Manufacturer
Preferred Pharmaceuticals, Inc

Identifiers & Regulatory

Product NDC 68788-7973
Product ID 68788-7973_f846731f-c3a8-4de0-8be6-d1bf34a2cb29
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040489
Listing Expiration 2026-12-31
Marketing Start 2021-07-28

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 687887973
Hyphenated Format 68788-7973

Supplemental Identifiers

RxCUI
197943
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 ANDA040489 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (68788-7973-3)
  • 60 TABLET in 1 BOTTLE (68788-7973-6)
  • 90 TABLET in 1 BOTTLE (68788-7973-9)
source: ndc

Packages (3)

68788-7973-3 30 TABLET in 1 BOTTLE (68788-7973-3) 68788-7973-6 60 TABLET in 1 BOTTLE (68788-7973-6) 68788-7973-9 90 TABLET in 1 BOTTLE (68788-7973-9)

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": "f846731f-c3a8-4de0-8be6-d1bf34a2cb29", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197943"], "spl_set_id": ["425abc3b-2111-4fac-bf27-b685d1e657af"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-7973-3)", "package_ndc": "68788-7973-3", "marketing_start_date": "20210728"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-7973-6)", "package_ndc": "68788-7973-6", "marketing_start_date": "20210728"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-7973-9)", "package_ndc": "68788-7973-9", "marketing_start_date": "20210728"}], "brand_name": "Methocarbamol", "product_id": "68788-7973_f846731f-c3a8-4de0-8be6-d1bf34a2cb29", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "68788-7973", "generic_name": "methocarbamol", "labeler_name": "Preferred Pharmaceuticals, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "500 mg/1"}], "application_number": "ANDA040489", "marketing_category": "ANDA", "marketing_start_date": "20210728", "listing_expiration_date": "20261231"}