methocarbamol

Generic: methocarbamol tablets

Labeler: granules india ltd
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methocarbamol
Generic Name methocarbamol tablets
Labeler granules india ltd
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

methocarbamol 500 mg/1

Manufacturer
Granules India Ltd

Identifiers & Regulatory

Product NDC 62207-754
Product ID 62207-754_44e3ccde-759c-0def-e063-6394a90ab87d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209312
Listing Expiration 2026-12-31
Marketing Start 2018-05-15

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 62207754
Hyphenated Format 62207-754

Supplemental Identifiers

RxCUI
197943 197944
UPC
0362207754491
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 tablets (source: ndc)
Application Number ANDA209312 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 24 TABLET, COATED in 1 BOTTLE (62207-754-41)
  • 100 TABLET, COATED in 1 BOTTLE (62207-754-43)
  • 500 TABLET, COATED in 1 BOTTLE (62207-754-47)
  • 1000 TABLET, COATED in 1 BOTTLE (62207-754-49)
source: ndc

Packages (4)

62207-754-41 24 TABLET, COATED in 1 BOTTLE (62207-754-41) 62207-754-43 100 TABLET, COATED in 1 BOTTLE (62207-754-43) 62207-754-47 500 TABLET, COATED in 1 BOTTLE (62207-754-47) 62207-754-49 1000 TABLET, COATED in 1 BOTTLE (62207-754-49)

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": "44e3ccde-759c-0def-e063-6394a90ab87d", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0362207754491"], "unii": ["125OD7737X"], "rxcui": ["197943", "197944"], "spl_set_id": ["42c0a177-7d62-4bcf-9fce-7dd484cda4d5"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Granules India Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 TABLET, COATED in 1 BOTTLE (62207-754-41)", "package_ndc": "62207-754-41", "marketing_start_date": "20180515"}, {"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (62207-754-43)", "package_ndc": "62207-754-43", "marketing_start_date": "20180515"}, {"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE (62207-754-47)", "package_ndc": "62207-754-47", "marketing_start_date": "20180515"}, {"sample": false, "description": "1000 TABLET, COATED in 1 BOTTLE (62207-754-49)", "package_ndc": "62207-754-49", "marketing_start_date": "20180515"}], "brand_name": "Methocarbamol", "product_id": "62207-754_44e3ccde-759c-0def-e063-6394a90ab87d", "dosage_form": "TABLET, COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "62207-754", "generic_name": "Methocarbamol Tablets", "labeler_name": "Granules India Ltd", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "500 mg/1"}], "application_number": "ANDA209312", "marketing_category": "ANDA", "marketing_start_date": "20180515", "listing_expiration_date": "20261231"}