methocarbamol

Generic: methocarbamol tablets

Labeler: granules pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methocarbamol
Generic Name methocarbamol tablets
Labeler granules pharmaceuticals inc.
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

methocarbamol 750 mg/1

Manufacturer
Granules Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 70010-770
Product ID 70010-770_31b78323-4baf-4af7-e063-6394a90a2c79
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209312
Listing Expiration 2026-12-31
Marketing Start 2018-07-02

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 70010770
Hyphenated Format 70010-770

Supplemental Identifiers

RxCUI
197943 197944
UPC
0370010754010 0370010770058
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
  • 750 mg/1
source: ndc
Packaging
  • 100 TABLET, COATED in 1 BOTTLE (70010-770-01)
  • 500 TABLET, COATED in 1 BOTTLE (70010-770-05)
source: ndc

Packages (2)

70010-770-01 100 TABLET, COATED in 1 BOTTLE (70010-770-01) 70010-770-05 500 TABLET, COATED in 1 BOTTLE (70010-770-05)

Ingredients (1)

methocarbamol (750 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": "31b78323-4baf-4af7-e063-6394a90a2c79", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0370010754010", "0370010770058"], "unii": ["125OD7737X"], "rxcui": ["197943", "197944"], "spl_set_id": ["6f0d3966-962d-fa7c-e053-2a91aa0a8e3c"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Granules Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (70010-770-01)", "package_ndc": "70010-770-01", "marketing_start_date": "20200201"}, {"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE (70010-770-05)", "package_ndc": "70010-770-05", "marketing_start_date": "20200201"}], "brand_name": "Methocarbamol", "product_id": "70010-770_31b78323-4baf-4af7-e063-6394a90a2c79", "dosage_form": "TABLET, COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "70010-770", "generic_name": "Methocarbamol Tablets", "labeler_name": "Granules Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "750 mg/1"}], "application_number": "ANDA209312", "marketing_category": "ANDA", "marketing_start_date": "20180702", "listing_expiration_date": "20261231"}