methocarbamol

Generic: methocarbamol tablets

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methocarbamol
Generic Name methocarbamol tablets
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

methocarbamol 500 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-903
Product ID 43063-903_32d385d8-7606-fee1-e063-6394a90a7a59
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 43063903
Hyphenated Format 43063-903

Supplemental Identifiers

RxCUI
197943
UPC
0343063903308
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
  • 500 mg/1
source: ndc
Packaging
  • 18 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-903-18)
  • 20 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-903-20)
  • 24 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-903-24)
  • 28 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-903-28)
  • 30 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-903-30)
source: ndc

Packages (5)

43063-903-18 18 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-903-18) 43063-903-20 20 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-903-20) 43063-903-24 24 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-903-24) 43063-903-28 28 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-903-28) 43063-903-30 30 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-903-30)

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": "32d385d8-7606-fee1-e063-6394a90a7a59", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0343063903308"], "unii": ["125OD7737X"], "rxcui": ["197943"], "spl_set_id": ["7dafab15-db4c-4425-b1a2-e56433ecccf6"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "18 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-903-18)", "package_ndc": "43063-903-18", "marketing_start_date": "20220502"}, {"sample": false, "description": "20 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-903-20)", "package_ndc": "43063-903-20", "marketing_start_date": "20181108"}, {"sample": false, "description": "24 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-903-24)", "package_ndc": "43063-903-24", "marketing_start_date": "20190225"}, {"sample": false, "description": "28 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-903-28)", "package_ndc": "43063-903-28", "marketing_start_date": "20181108"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-903-30)", "package_ndc": "43063-903-30", "marketing_start_date": "20181114"}], "brand_name": "Methocarbamol", "product_id": "43063-903_32d385d8-7606-fee1-e063-6394a90a7a59", "dosage_form": "TABLET, COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "43063-903", "generic_name": "Methocarbamol Tablets", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "500 mg/1"}], "application_number": "ANDA209312", "marketing_category": "ANDA", "marketing_start_date": "20180702", "listing_expiration_date": "20261231"}