methocarbamol

Generic: methocarbamol tablets

Labeler: mckesson corporation dba sky packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methocarbamol
Generic Name methocarbamol tablets
Labeler mckesson corporation dba sky packaging
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

methocarbamol 750 mg/1

Manufacturer
McKesson Corporation dba SKY Packaging

Identifiers & Regulatory

Product NDC 63739-992
Product ID 63739-992_2b39b36a-a3b4-f6a3-e063-6294a90aa9ed
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209312
Marketing Start 2021-07-22
Marketing End 2026-03-31

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 63739992
Hyphenated Format 63739-992

Supplemental Identifiers

RxCUI
197943 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
  • 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-992-10) / 10 TABLET, COATED in 1 BLISTER PACK
source: ndc

Packages (1)

63739-992-10 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-992-10) / 10 TABLET, COATED in 1 BLISTER PACK

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": "2b39b36a-a3b4-f6a3-e063-6294a90aa9ed", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197943", "197944"], "spl_set_id": ["c7bc1e92-28cb-31ae-e053-2a95a90aeb3f"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["McKesson Corporation dba SKY Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-992-10)  / 10 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "63739-992-10", "marketing_end_date": "20260331", "marketing_start_date": "20210722"}], "brand_name": "Methocarbamol", "product_id": "63739-992_2b39b36a-a3b4-f6a3-e063-6294a90aa9ed", "dosage_form": "TABLET, COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "63739-992", "generic_name": "Methocarbamol Tablets", "labeler_name": "McKesson Corporation dba SKY Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "750 mg/1"}], "application_number": "ANDA209312", "marketing_category": "ANDA", "marketing_end_date": "20260331", "marketing_start_date": "20210722"}