methocarbamol

Generic: methocarbamol tablets

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

Drug Facts

Product Profile

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

methocarbamol 500 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-4520
Product ID 68071-4520_49a0a91a-ad87-d1f7-e063-6294a90a6bcc
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 680714520
Hyphenated Format 68071-4520

Supplemental Identifiers

RxCUI
197943
UPC
0368071452037
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
  • 20 TABLET, COATED in 1 BOTTLE (68071-4520-2)
  • 30 TABLET, COATED in 1 BOTTLE (68071-4520-3)
  • 60 TABLET, COATED in 1 BOTTLE (68071-4520-6)
  • 90 TABLET, COATED in 1 BOTTLE (68071-4520-9)
source: ndc

Packages (4)

68071-4520-2 20 TABLET, COATED in 1 BOTTLE (68071-4520-2) 68071-4520-3 30 TABLET, COATED in 1 BOTTLE (68071-4520-3) 68071-4520-6 60 TABLET, COATED in 1 BOTTLE (68071-4520-6) 68071-4520-9 90 TABLET, COATED in 1 BOTTLE (68071-4520-9)

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": "49a0a91a-ad87-d1f7-e063-6294a90a6bcc", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0368071452037"], "unii": ["125OD7737X"], "rxcui": ["197943"], "spl_set_id": ["72f36d28-15d2-30f6-e053-2a91aa0ad1ce"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, COATED in 1 BOTTLE (68071-4520-2)", "package_ndc": "68071-4520-2", "marketing_start_date": "20180808"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (68071-4520-3)", "package_ndc": "68071-4520-3", "marketing_start_date": "20180808"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (68071-4520-6)", "package_ndc": "68071-4520-6", "marketing_start_date": "20250114"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (68071-4520-9)", "package_ndc": "68071-4520-9", "marketing_start_date": "20260130"}], "brand_name": "Methocarbamol", "product_id": "68071-4520_49a0a91a-ad87-d1f7-e063-6294a90a6bcc", "dosage_form": "TABLET, COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "68071-4520", "generic_name": "Methocarbamol Tablets", "labeler_name": "NuCare Pharmaceuticals,Inc.", "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"}