tramadol hydrochloride

Generic: tramadol hydrochloride

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

Drug Facts

Product Profile

Brand Name tramadol hydrochloride
Generic Name tramadol hydrochloride
Labeler nucare pharmaceuticals,inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

tramadol hydrochloride 50 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-5204
Product ID 68071-5204_1b56f30a-701f-112e-e063-6294a90a2c14
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075964
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2002-06-22

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680715204
Hyphenated Format 68071-5204

Supplemental Identifiers

RxCUI
835603
UPC
0368071520439
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 ANDA075964 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (68071-5204-3)
  • 40 TABLET in 1 BOTTLE (68071-5204-4)
  • 15 TABLET in 1 BOTTLE (68071-5204-5)
  • 180 TABLET in 1 BOTTLE (68071-5204-8)
  • 90 TABLET in 1 BOTTLE (68071-5204-9)
source: ndc

Packages (5)

68071-5204-3 30 TABLET in 1 BOTTLE (68071-5204-3) 68071-5204-4 40 TABLET in 1 BOTTLE (68071-5204-4) 68071-5204-5 15 TABLET in 1 BOTTLE (68071-5204-5) 68071-5204-8 180 TABLET in 1 BOTTLE (68071-5204-8) 68071-5204-9 90 TABLET in 1 BOTTLE (68071-5204-9)

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": "1b56f30a-701f-112e-e063-6294a90a2c14", "openfda": {"upc": ["0368071520439"], "unii": ["9N7R477WCK"], "rxcui": ["835603"], "spl_set_id": ["a0ad984a-38da-1fe0-e053-2995a90af23e"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-5204-3)", "package_ndc": "68071-5204-3", "marketing_start_date": "20200312"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (68071-5204-4)", "package_ndc": "68071-5204-4", "marketing_start_date": "20200312"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (68071-5204-5)", "package_ndc": "68071-5204-5", "marketing_start_date": "20200312"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (68071-5204-8)", "package_ndc": "68071-5204-8", "marketing_start_date": "20200312"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-5204-9)", "package_ndc": "68071-5204-9", "marketing_start_date": "20200312"}], "brand_name": "tramadol hydrochloride", "product_id": "68071-5204_1b56f30a-701f-112e-e063-6294a90a2c14", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "68071-5204", "dea_schedule": "CIV", "generic_name": "tramadol hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "tramadol hydrochloride", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA075964", "marketing_category": "ANDA", "marketing_start_date": "20020622", "listing_expiration_date": "20261231"}