methocarbamol

Generic: methocarbamol

Labeler: bostal llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methocarbamol
Generic Name methocarbamol
Labeler bostal llc
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

methocarbamol 500 mg/1

Manufacturer
Bostal LLC

Identifiers & Regulatory

Product NDC 35561-212
Product ID 35561-212_49fcc548-27fe-58d0-e063-6294a90af96d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200958
Listing Expiration 2027-12-31
Marketing Start 2018-10-10

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 35561212
Hyphenated Format 35561-212

Supplemental Identifiers

RxCUI
197943 197944 2611794
UPC
0335561212129 0335561211122 0335561349122 0335561349139 0335561211139 0335561212136
UNII
125OD7737X
NUI
N0000175730 N0000175737

Packaging Origin

Original Packager
true

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 ANDA200958 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 100 TABLET, COATED in 1 BOTTLE, PLASTIC (35561-212-12)
  • 500 TABLET, COATED in 1 BOTTLE, PLASTIC (35561-212-13)
source: ndc

Packages (2)

35561-212-12 100 TABLET, COATED in 1 BOTTLE, PLASTIC (35561-212-12) 35561-212-13 500 TABLET, COATED in 1 BOTTLE, PLASTIC (35561-212-13)

Ingredients (1)

methocarbamol (500 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": "49fcc548-27fe-58d0-e063-6294a90af96d", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0335561212129", "0335561211122", "0335561349122", "0335561349139", "0335561211139", "0335561212136"], "unii": ["125OD7737X"], "rxcui": ["197943", "197944", "2611794"], "spl_set_id": ["d8f10211-f96e-4cf3-9b49-986eb51b703d"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Bostal LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE, PLASTIC (35561-212-12)", "package_ndc": "35561-212-12", "marketing_start_date": "20181010"}, {"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE, PLASTIC (35561-212-13)", "package_ndc": "35561-212-13", "marketing_start_date": "20181010"}], "brand_name": "Methocarbamol", "product_id": "35561-212_49fcc548-27fe-58d0-e063-6294a90af96d", "dosage_form": "TABLET, COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "35561-212", "generic_name": "Methocarbamol", "labeler_name": "Bostal LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "500 mg/1"}], "application_number": "ANDA200958", "marketing_category": "ANDA", "marketing_start_date": "20181010", "listing_expiration_date": "20271231"}