methocarbamol

Generic: methocarbamol tablets

Labeler: redpharm drug
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methocarbamol
Generic Name methocarbamol tablets
Labeler redpharm drug
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

methocarbamol 500 mg/1

Manufacturer
Redpharm Drug

Identifiers & Regulatory

Product NDC 67296-2197
Product ID 67296-2197_4c446b06-eba3-8fe1-e063-6294a90aa8b4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209312
Listing Expiration 2027-12-31
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 672962197
Hyphenated Format 67296-2197

Supplemental Identifiers

RxCUI
197943
UPC
0370010754010 0370010770058
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 tablets (source: ndc)
Application Number ANDA209312 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 15 TABLET, COATED in 1 BOTTLE (67296-2197-1)
  • 40 TABLET, COATED in 1 BOTTLE (67296-2197-2)
  • 30 TABLET, COATED in 1 BOTTLE (67296-2197-3)
source: ndc

Packages (3)

67296-2197-1 15 TABLET, COATED in 1 BOTTLE (67296-2197-1) 67296-2197-2 40 TABLET, COATED in 1 BOTTLE (67296-2197-2) 67296-2197-3 30 TABLET, COATED in 1 BOTTLE (67296-2197-3)

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": "4c446b06-eba3-8fe1-e063-6294a90aa8b4", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0370010754010", "0370010770058"], "unii": ["125OD7737X"], "rxcui": ["197943"], "spl_set_id": ["44f264fd-bf40-bed9-e063-6294a90ac44a"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, COATED in 1 BOTTLE (67296-2197-1)", "package_ndc": "67296-2197-1", "marketing_start_date": "20200201"}, {"sample": false, "description": "40 TABLET, COATED in 1 BOTTLE (67296-2197-2)", "package_ndc": "67296-2197-2", "marketing_start_date": "20200201"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (67296-2197-3)", "package_ndc": "67296-2197-3", "marketing_start_date": "20200201"}], "brand_name": "Methocarbamol", "product_id": "67296-2197_4c446b06-eba3-8fe1-e063-6294a90aa8b4", "dosage_form": "TABLET, COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "67296-2197", "generic_name": "Methocarbamol Tablets", "labeler_name": "Redpharm Drug", "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": "20180702", "listing_expiration_date": "20271231"}