methocarbamol
Generic: methocarbamol
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
methocarbamol
Generic Name
methocarbamol
Labeler
proficient rx lp
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
methocarbamol 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71205-103
Product ID
71205-103_185894ce-3da6-4a5b-83e6-daeba7b3c362
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208507
Listing Expiration
2026-12-31
Marketing Start
2018-01-15
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71205103
Hyphenated Format
71205-103
Supplemental Identifiers
RxCUI
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
- 20 TABLET, FILM COATED in 1 BOTTLE (71205-103-20)
- 30 TABLET, FILM COATED in 1 BOTTLE (71205-103-30)
- 40 TABLET, FILM COATED in 1 BOTTLE (71205-103-40)
- 45 TABLET, FILM COATED in 1 BOTTLE (71205-103-45)
- 60 TABLET, FILM COATED in 1 BOTTLE (71205-103-60)
- 90 TABLET, FILM COATED in 1 BOTTLE (71205-103-90)
Packages (6)
71205-103-20
20 TABLET, FILM COATED in 1 BOTTLE (71205-103-20)
71205-103-30
30 TABLET, FILM COATED in 1 BOTTLE (71205-103-30)
71205-103-40
40 TABLET, FILM COATED in 1 BOTTLE (71205-103-40)
71205-103-45
45 TABLET, FILM COATED in 1 BOTTLE (71205-103-45)
71205-103-60
60 TABLET, FILM COATED in 1 BOTTLE (71205-103-60)
71205-103-90
90 TABLET, FILM COATED in 1 BOTTLE (71205-103-90)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "185894ce-3da6-4a5b-83e6-daeba7b3c362", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197943"], "spl_set_id": ["39b4362e-a26e-49cb-9d06-898bc9b0e005"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (71205-103-20)", "package_ndc": "71205-103-20", "marketing_start_date": "20180904"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-103-30)", "package_ndc": "71205-103-30", "marketing_start_date": "20180904"}, {"sample": false, "description": "40 TABLET, FILM COATED in 1 BOTTLE (71205-103-40)", "package_ndc": "71205-103-40", "marketing_start_date": "20180904"}, {"sample": false, "description": "45 TABLET, FILM COATED in 1 BOTTLE (71205-103-45)", "package_ndc": "71205-103-45", "marketing_start_date": "20180904"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-103-60)", "package_ndc": "71205-103-60", "marketing_start_date": "20180904"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-103-90)", "package_ndc": "71205-103-90", "marketing_start_date": "20180904"}], "brand_name": "Methocarbamol", "product_id": "71205-103_185894ce-3da6-4a5b-83e6-daeba7b3c362", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "71205-103", "generic_name": "Methocarbamol", "labeler_name": "Proficient Rx LP", "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": "20261231"}