tramadol hydrochloride

Generic: tramadol hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tramadol hydrochloride
Generic Name tramadol hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

tramadol hydrochloride 200 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1676
Product ID 71335-1676_6da94891-d49c-4fab-ba67-1a585a385be9
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 713351676
Hyphenated Format 71335-1676

Supplemental Identifiers

RxCUI
833711
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 (71335-1676-1)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1676-2)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1676-3)
  • 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1676-4)
source: ndc

Packages (4)

71335-1676-1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1676-1) 71335-1676-2 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1676-2) 71335-1676-3 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1676-3) 71335-1676-4 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1676-4)

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": "6da94891-d49c-4fab-ba67-1a585a385be9", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["833711"], "spl_set_id": ["66359f41-9999-4cb8-b632-1fe2ec1e60b2"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1676-1)", "package_ndc": "71335-1676-1", "marketing_start_date": "20200710"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1676-2)", "package_ndc": "71335-1676-2", "marketing_start_date": "20200708"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1676-3)", "package_ndc": "71335-1676-3", "marketing_start_date": "20200813"}, {"sample": false, "description": "120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1676-4)", "package_ndc": "71335-1676-4", "marketing_start_date": "20240404"}], "brand_name": "TRAMADOL HYDROCHLORIDE", "product_id": "71335-1676_6da94891-d49c-4fab-ba67-1a585a385be9", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "71335-1676", "dea_schedule": "CIV", "generic_name": "TRAMADOL HYDROCHLORIDE", "labeler_name": "Bryant Ranch Prepack", "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"}