methocarbamol

Generic: methocarbamol

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methocarbamol
Generic Name methocarbamol
Labeler american health packaging
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methocarbamol 750 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-568
Product ID 60687-568_22058b66-8c4a-4a0b-e063-6394a90ae73e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090200
Listing Expiration 2026-12-31
Marketing Start 2020-05-20

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 60687568
Hyphenated Format 60687-568

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 (source: ndc)
Application Number ANDA090200 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-568-01) / 1 TABLET in 1 BLISTER PACK (60687-568-11)
source: ndc

Packages (1)

60687-568-01 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-568-01) / 1 TABLET in 1 BLISTER PACK (60687-568-11)

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": "22058b66-8c4a-4a0b-e063-6394a90ae73e", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197943", "197944"], "spl_set_id": ["d842fe4e-fc46-4d70-9ca3-b47191672f96"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-568-01)  / 1 TABLET in 1 BLISTER PACK (60687-568-11)", "package_ndc": "60687-568-01", "marketing_start_date": "20200520"}], "brand_name": "Methocarbamol", "product_id": "60687-568_22058b66-8c4a-4a0b-e063-6394a90ae73e", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "60687-568", "generic_name": "Methocarbamol", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "750 mg/1"}], "application_number": "ANDA090200", "marketing_category": "ANDA", "marketing_start_date": "20200520", "listing_expiration_date": "20261231"}