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 750 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-905
Product ID 43063-905_32d38d53-d181-0b14-e063-6394a90ae577
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 43063905
Hyphenated Format 43063-905

Supplemental Identifiers

RxCUI
197944
UPC
0343063905302
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
  • 14 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-905-14)
  • 20 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-905-20)
  • 30 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-905-30)
  • 40 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-905-40)
  • 60 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-905-60)
source: ndc

Packages (5)

43063-905-14 14 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-905-14) 43063-905-20 20 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-905-20) 43063-905-30 30 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-905-30) 43063-905-40 40 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-905-40) 43063-905-60 60 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-905-60)

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": "32d38d53-d181-0b14-e063-6394a90ae577", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0343063905302"], "unii": ["125OD7737X"], "rxcui": ["197944"], "spl_set_id": ["d0acdf52-e1a9-4489-91e1-ef434d311613"], "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": "14 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-905-14)", "package_ndc": "43063-905-14", "marketing_start_date": "20181108"}, {"sample": false, "description": "20 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-905-20)", "package_ndc": "43063-905-20", "marketing_start_date": "20181108"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-905-30)", "package_ndc": "43063-905-30", "marketing_start_date": "20181108"}, {"sample": false, "description": "40 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-905-40)", "package_ndc": "43063-905-40", "marketing_start_date": "20181112"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-905-60)", "package_ndc": "43063-905-60", "marketing_start_date": "20190109"}], "brand_name": "Methocarbamol", "product_id": "43063-905_32d38d53-d181-0b14-e063-6394a90ae577", "dosage_form": "TABLET, COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "43063-905", "generic_name": "Methocarbamol Tablets", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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"}