tramadol hydrochloride

Generic: tramadol hydrochloride

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

Drug Facts

Product Profile

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

tramadol hydrochloride 50 mg/1

Manufacturer
RedPharm Drug, Inc.

Identifiers & Regulatory

Product NDC 67296-1021
Product ID 67296-1021_1cfead90-c8e9-3bb3-e063-6394a90a1090
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 672961021
Hyphenated Format 67296-1021

Supplemental Identifiers

RxCUI
835603
UPC
0367296102178 0367296102154
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
  • 10 TABLET in 1 BOTTLE (67296-1021-1)
  • 20 TABLET in 1 BOTTLE (67296-1021-2)
  • 30 TABLET in 1 BOTTLE (67296-1021-3)
  • 45 TABLET in 1 BOTTLE (67296-1021-4)
  • 15 TABLET in 1 BOTTLE (67296-1021-5)
  • 6 TABLET in 1 BOTTLE (67296-1021-6)
  • 40 TABLET in 1 BOTTLE (67296-1021-7)
source: ndc

Packages (7)

Ingredients (1)

tramadol hydrochloride (50 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1cfead90-c8e9-3bb3-e063-6394a90a1090", "openfda": {"upc": ["0367296102178", "0367296102154"], "unii": ["9N7R477WCK"], "rxcui": ["835603"], "spl_set_id": ["4e2c0893-6faf-15ed-e054-00144ff8d46c"], "manufacturer_name": ["RedPharm Drug, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (67296-1021-1)", "package_ndc": "67296-1021-1", "marketing_start_date": "20020622"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (67296-1021-2)", "package_ndc": "67296-1021-2", "marketing_start_date": "20210101"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (67296-1021-3)", "package_ndc": "67296-1021-3", "marketing_start_date": "20020622"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE (67296-1021-4)", "package_ndc": "67296-1021-4", "marketing_start_date": "20020622"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (67296-1021-5)", "package_ndc": "67296-1021-5", "marketing_start_date": "20020622"}, {"sample": false, "description": "6 TABLET in 1 BOTTLE (67296-1021-6)", "package_ndc": "67296-1021-6", "marketing_start_date": "20020622"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (67296-1021-7)", "package_ndc": "67296-1021-7", "marketing_start_date": "20210101"}], "brand_name": "tramadol hydrochloride", "product_id": "67296-1021_1cfead90-c8e9-3bb3-e063-6394a90a1090", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "67296-1021", "dea_schedule": "CIV", "generic_name": "tramadol hydrochloride", "labeler_name": "RedPharm Drug, 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"}