methocarbamol
Generic: methocarbamol
Labeler: camber pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
methocarbamol
Generic Name
methocarbamol
Labeler
camber pharmaceuticals, inc.
Dosage Form
TABLET
Routes
Active Ingredients
methocarbamol 750 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
31722-534
Product ID
31722-534_bf48c1c6-3723-1fde-e053-2995a90af824
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090200
Listing Expiration
2026-12-31
Marketing Start
2013-03-20
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
31722534
Hyphenated Format
31722-534
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 750 mg/1
Packaging
- 12 BOTTLE in 1 CASE (31722-534-01) / 100 TABLET in 1 BOTTLE
- 12 BOTTLE in 1 CASE (31722-534-05) / 500 TABLET in 1 BOTTLE
- 12 BOTTLE in 1 CASE (31722-534-30) / 30 TABLET in 1 BOTTLE
- 12 BOTTLE in 1 CASE (31722-534-60) / 60 TABLET in 1 BOTTLE
Packages (4)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "bf48c1c6-3723-1fde-e053-2995a90af824", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0331722534307", "0331722533300"], "unii": ["125OD7737X"], "rxcui": ["197943", "197944"], "spl_set_id": ["43af0c41-9990-4902-9384-75de5ea08283"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 BOTTLE in 1 CASE (31722-534-01) / 100 TABLET in 1 BOTTLE", "package_ndc": "31722-534-01", "marketing_start_date": "20130320"}, {"sample": false, "description": "12 BOTTLE in 1 CASE (31722-534-05) / 500 TABLET in 1 BOTTLE", "package_ndc": "31722-534-05", "marketing_start_date": "20130320"}, {"sample": false, "description": "12 BOTTLE in 1 CASE (31722-534-30) / 30 TABLET in 1 BOTTLE", "package_ndc": "31722-534-30", "marketing_start_date": "20130320"}, {"sample": false, "description": "12 BOTTLE in 1 CASE (31722-534-60) / 60 TABLET in 1 BOTTLE", "package_ndc": "31722-534-60", "marketing_start_date": "20130320"}], "brand_name": "Methocarbamol", "product_id": "31722-534_bf48c1c6-3723-1fde-e053-2995a90af824", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "31722-534", "generic_name": "Methocarbamol", "labeler_name": "Camber Pharmaceuticals, Inc.", "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": "20130320", "listing_expiration_date": "20261231"}