methocarbamol

Generic: methocarbamol

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methocarbamol
Generic Name methocarbamol
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methocarbamol 750 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-398
Product ID 72789-398_4123336c-9e83-3a81-e063-6394a90aed54
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040489
Listing Expiration 2026-12-31
Marketing Start 2019-08-15

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 72789398
Hyphenated Format 72789-398

Supplemental Identifiers

RxCUI
197944
UPC
0372789398822
UNII
125OD7737X
NUI
N0000175730 N0000175737

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 ANDA040489 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (72789-398-01)
  • 500 TABLET in 1 BOTTLE, PLASTIC (72789-398-82)
source: ndc

Packages (2)

72789-398-01 100 TABLET in 1 BOTTLE, PLASTIC (72789-398-01) 72789-398-82 500 TABLET in 1 BOTTLE, PLASTIC (72789-398-82)

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": "4123336c-9e83-3a81-e063-6394a90aed54", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0372789398822"], "unii": ["125OD7737X"], "rxcui": ["197944"], "spl_set_id": ["3d4a2486-863e-4e9f-be3b-67882863e7d4"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72789-398-01)", "package_ndc": "72789-398-01", "marketing_start_date": "20240507"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (72789-398-82)", "package_ndc": "72789-398-82", "marketing_start_date": "20240507"}], "brand_name": "Methocarbamol", "product_id": "72789-398_4123336c-9e83-3a81-e063-6394a90aed54", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "72789-398", "generic_name": "methocarbamol", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "750 mg/1"}], "application_number": "ANDA040489", "marketing_category": "ANDA", "marketing_start_date": "20190815", "listing_expiration_date": "20261231"}