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 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72789-012
Product ID
72789-012_4af2fbb0-4343-0414-e063-6294a90aa54c
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
72789012
Hyphenated Format
72789-012
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
- 500 mg/1
Packaging
- 18 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-18)
- 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-20)
- 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-24)
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-30)
- 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-40)
Packages (5)
72789-012-18
18 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-18)
72789-012-20
20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-20)
72789-012-24
24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-24)
72789-012-30
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-30)
72789-012-40
40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-40)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4af2fbb0-4343-0414-e063-6294a90aa54c", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0372789012308"], "unii": ["125OD7737X"], "rxcui": ["197943"], "spl_set_id": ["288a3bcd-a2c8-4a9b-9602-59c0493b4a8d"], "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, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-18)", "package_ndc": "72789-012-18", "marketing_start_date": "20191219"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-20)", "package_ndc": "72789-012-20", "marketing_start_date": "20190920"}, {"sample": false, "description": "24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-24)", "package_ndc": "72789-012-24", "marketing_start_date": "20210505"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-30)", "package_ndc": "72789-012-30", "marketing_start_date": "20210810"}, {"sample": false, "description": "40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-40)", "package_ndc": "72789-012-40", "marketing_start_date": "20200616"}], "brand_name": "Methocarbamol", "product_id": "72789-012_4af2fbb0-4343-0414-e063-6294a90aa54c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "72789-012", "generic_name": "Methocarbamol", "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": "ANDA208507", "marketing_category": "ANDA", "marketing_start_date": "20180115", "listing_expiration_date": "20271231"}