tramadol hydrochloride

Generic: tramadol hydrochloride

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tramadol hydrochloride
Generic Name tramadol hydrochloride
Labeler proficient rx lp
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

tramadol hydrochloride 200 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-708
Product ID 71205-708_00b7f61b-5173-43e6-a3f9-d2efbda40c19
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA201384
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2011-12-12

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205708
Hyphenated Format 71205-708

Supplemental Identifiers

RxCUI
833711
UPC
0371205708306
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 ANDA201384 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-708-30)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-708-60)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-708-90)
source: ndc

Packages (3)

71205-708-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-708-30) 71205-708-60 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-708-60) 71205-708-90 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-708-90)

Ingredients (1)

tramadol hydrochloride (200 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": "00b7f61b-5173-43e6-a3f9-d2efbda40c19", "openfda": {"upc": ["0371205708306"], "unii": ["9N7R477WCK"], "rxcui": ["833711"], "spl_set_id": ["00b7f61b-5173-43e6-a3f9-d2efbda40c19"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-708-30)", "package_ndc": "71205-708-30", "marketing_start_date": "20221031"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-708-60)", "package_ndc": "71205-708-60", "marketing_start_date": "20221031"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-708-90)", "package_ndc": "71205-708-90", "marketing_start_date": "20221031"}], "brand_name": "TRAMADOL HYDROCHLORIDE", "product_id": "71205-708_00b7f61b-5173-43e6-a3f9-d2efbda40c19", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "71205-708", "dea_schedule": "CIV", "generic_name": "TRAMADOL HYDROCHLORIDE", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRAMADOL HYDROCHLORIDE", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA201384", "marketing_category": "ANDA", "marketing_start_date": "20111212", "listing_expiration_date": "20261231"}