tramadol hydrochloride

Generic: tramadol hydrochloride

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

Drug Facts

Product Profile

Brand Name tramadol hydrochloride
Generic Name tramadol hydrochloride
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

tramadol hydrochloride 50 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4248
Product ID 70518-4248_4007fbf6-8ef0-85e9-e063-6394a90a4013
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202075
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2024-12-30

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705184248
Hyphenated Format 70518-4248

Supplemental Identifiers

RxCUI
835603
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 ANDA202075 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BLISTER PACK (70518-4248-0)
source: ndc

Packages (1)

70518-4248-0 30 TABLET in 1 BLISTER PACK (70518-4248-0)

Ingredients (1)

tramadol hydrochloride (50 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": "4007fbf6-8ef0-85e9-e063-6394a90a4013", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["835603"], "spl_set_id": ["c6104e62-5b2c-41a1-afb3-00dcf267a384"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4248-0)", "package_ndc": "70518-4248-0", "marketing_start_date": "20241230"}], "brand_name": "tramadol hydrochloride", "product_id": "70518-4248_4007fbf6-8ef0-85e9-e063-6394a90a4013", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "70518-4248", "dea_schedule": "CIV", "generic_name": "tramadol hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "tramadol hydrochloride", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA202075", "marketing_category": "ANDA", "marketing_start_date": "20241230", "listing_expiration_date": "20261231"}