methocarbamol
Generic: methocarbamol
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
methocarbamol
Generic Name
methocarbamol
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
methocarbamol 750 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72789-022
Product ID
72789-022_4af2ff79-e0d9-6484-e063-6394a90ad124
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208507
Listing Expiration
2027-12-31
Marketing Start
2018-01-15
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72789022
Hyphenated Format
72789-022
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
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
ANDA208507 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 750 mg/1
Packaging
- 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-01)
- 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-82)
- 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-90)
- 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-93)
- 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-98)
Packages (5)
72789-022-01
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-01)
72789-022-82
500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-82)
72789-022-90
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-90)
72789-022-93
180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-93)
72789-022-98
120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-98)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4af2ff79-e0d9-6484-e063-6394a90ad124", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0372789022826"], "unii": ["125OD7737X"], "rxcui": ["197944"], "spl_set_id": ["3b0e60a7-3cff-4665-a473-ad3257619cdd"], "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": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-01)", "package_ndc": "72789-022-01", "marketing_start_date": "20191024"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-82)", "package_ndc": "72789-022-82", "marketing_start_date": "20191024"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-90)", "package_ndc": "72789-022-90", "marketing_start_date": "20230912"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-93)", "package_ndc": "72789-022-93", "marketing_start_date": "20230912"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-98)", "package_ndc": "72789-022-98", "marketing_start_date": "20230912"}], "brand_name": "Methocarbamol", "product_id": "72789-022_4af2ff79-e0d9-6484-e063-6394a90ad124", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "72789-022", "generic_name": "Methocarbamol", "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": "ANDA208507", "marketing_category": "ANDA", "marketing_start_date": "20180115", "listing_expiration_date": "20271231"}