tramadol hydrochloride

Generic: tramadol hydrochloride

Labeler: coupler llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tramadol hydrochloride
Generic Name tramadol hydrochloride
Labeler coupler llc
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

tramadol hydrochloride 100 mg/1

Manufacturer
Coupler LLC

Identifiers & Regulatory

Product NDC 67046-1541
Product ID 67046-1541_3135a0e3-6e29-4091-e063-6394a90a52cb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208708
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2025-03-25

Pharmacologic Class

Classes
full opioid agonists [moa] opioid agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 670461541
Hyphenated Format 67046-1541

Supplemental Identifiers

RxCUI
2179635
UNII
9N7R477WCK

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 tramadol hydrochloride (source: ndc)
Generic Name tramadol hydrochloride (source: ndc)
Application Number ANDA208708 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 TABLET, COATED in 1 BLISTER PACK (67046-1541-3)
source: ndc

Packages (1)

67046-1541-3 30 TABLET, COATED in 1 BLISTER PACK (67046-1541-3)

Ingredients (1)

tramadol hydrochloride (100 mg/1)

Linked Drug Pages (1)

Tramadol Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3135a0e3-6e29-4091-e063-6394a90a52cb", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["2179635"], "spl_set_id": ["3135a131-5f2d-3775-e063-6394a90a4322"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BLISTER PACK (67046-1541-3)", "package_ndc": "67046-1541-3", "marketing_start_date": "20250325"}], "brand_name": "Tramadol Hydrochloride", "product_id": "67046-1541_3135a0e3-6e29-4091-e063-6394a90a52cb", "dosage_form": "TABLET, COATED", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "67046-1541", "dea_schedule": "CIV", "generic_name": "Tramadol Hydrochloride", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tramadol Hydrochloride", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA208708", "marketing_category": "ANDA", "marketing_start_date": "20250325", "listing_expiration_date": "20261231"}