tramadol hydrochloride
Generic: tramadol hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
tramadol hydrochloride
Generic Name
tramadol hydrochloride
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
tramadol hydrochloride 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-0521
Product ID
71335-0521_effdd857-cee6-4be6-8c91-66d2b9dcec59
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713350521
Hyphenated Format
71335-0521
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 50 TABLET in 1 BOTTLE (71335-0521-0)
- 30 TABLET in 1 BOTTLE (71335-0521-1)
- 20 TABLET in 1 BOTTLE (71335-0521-2)
- 90 TABLET in 1 BOTTLE (71335-0521-3)
- 60 TABLET in 1 BOTTLE (71335-0521-4)
- 120 TABLET in 1 BOTTLE (71335-0521-5)
- 180 TABLET in 1 BOTTLE (71335-0521-6)
- 40 TABLET in 1 BOTTLE (71335-0521-7)
- 100 TABLET in 1 BOTTLE (71335-0521-8)
- 15 TABLET in 1 BOTTLE (71335-0521-9)
Packages (10)
71335-0521-0
50 TABLET in 1 BOTTLE (71335-0521-0)
71335-0521-1
30 TABLET in 1 BOTTLE (71335-0521-1)
71335-0521-2
20 TABLET in 1 BOTTLE (71335-0521-2)
71335-0521-3
90 TABLET in 1 BOTTLE (71335-0521-3)
71335-0521-4
60 TABLET in 1 BOTTLE (71335-0521-4)
71335-0521-5
120 TABLET in 1 BOTTLE (71335-0521-5)
71335-0521-6
180 TABLET in 1 BOTTLE (71335-0521-6)
71335-0521-7
40 TABLET in 1 BOTTLE (71335-0521-7)
71335-0521-8
100 TABLET in 1 BOTTLE (71335-0521-8)
71335-0521-9
15 TABLET in 1 BOTTLE (71335-0521-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "effdd857-cee6-4be6-8c91-66d2b9dcec59", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["835603"], "spl_set_id": ["b2575a24-b0d9-470b-9b82-625deaf83c00"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET in 1 BOTTLE (71335-0521-0)", "package_ndc": "71335-0521-0", "marketing_start_date": "20190212"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0521-1)", "package_ndc": "71335-0521-1", "marketing_start_date": "20181214"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71335-0521-2)", "package_ndc": "71335-0521-2", "marketing_start_date": "20190111"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0521-3)", "package_ndc": "71335-0521-3", "marketing_start_date": "20181212"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-0521-4)", "package_ndc": "71335-0521-4", "marketing_start_date": "20181212"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-0521-5)", "package_ndc": "71335-0521-5", "marketing_start_date": "20181203"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71335-0521-6)", "package_ndc": "71335-0521-6", "marketing_start_date": "20181127"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (71335-0521-7)", "package_ndc": "71335-0521-7", "marketing_start_date": "20190531"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-0521-8)", "package_ndc": "71335-0521-8", "marketing_start_date": "20190129"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (71335-0521-9)", "package_ndc": "71335-0521-9", "marketing_start_date": "20190211"}], "brand_name": "tramadol hydrochloride", "product_id": "71335-0521_effdd857-cee6-4be6-8c91-66d2b9dcec59", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "71335-0521", "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": "50 mg/1"}], "application_number": "ANDA075964", "marketing_category": "ANDA", "marketing_start_date": "20020622", "listing_expiration_date": "20261231"}