tramadol hydrochloride
Generic: tramadol hydrochloride
Labeler: redpharm drug incDrug Facts
Product Profile
Brand Name
tramadol hydrochloride
Generic Name
tramadol hydrochloride
Labeler
redpharm drug inc
Dosage Form
TABLET, COATED
Routes
Active Ingredients
tramadol hydrochloride 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
67296-1834
Product ID
67296-1834_4387f592-853f-01ea-e063-6394a90a6a4f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208708
DEA Schedule
civ
Listing Expiration
2026-12-31
Marketing Start
2021-04-22
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
672961834
Hyphenated Format
67296-1834
Supplemental Identifiers
RxCUI
UPC
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
ANDA208708 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 10 TABLET, COATED in 1 BOTTLE (67296-1834-1)
- 20 TABLET, COATED in 1 BOTTLE (67296-1834-2)
- 30 TABLET, COATED in 1 BOTTLE (67296-1834-3)
- 40 TABLET, COATED in 1 BOTTLE (67296-1834-4)
- 6 TABLET, COATED in 1 BOTTLE (67296-1834-6)
- 15 TABLET, COATED in 1 BOTTLE (67296-1834-7)
Packages (6)
67296-1834-1
10 TABLET, COATED in 1 BOTTLE (67296-1834-1)
67296-1834-2
20 TABLET, COATED in 1 BOTTLE (67296-1834-2)
67296-1834-3
30 TABLET, COATED in 1 BOTTLE (67296-1834-3)
67296-1834-4
40 TABLET, COATED in 1 BOTTLE (67296-1834-4)
67296-1834-6
6 TABLET, COATED in 1 BOTTLE (67296-1834-6)
67296-1834-7
15 TABLET, COATED in 1 BOTTLE (67296-1834-7)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4387f592-853f-01ea-e063-6394a90a6a4f", "openfda": {"upc": ["0372888080017", "0372888080000", "0372888008011", "0372888008004", "0372888080055", "0372888008059"], "unii": ["9N7R477WCK"], "rxcui": ["835603"], "spl_set_id": ["f4c148f3-845a-61e3-e053-2a95a90a326e"], "manufacturer_name": ["RedPharm Drug Inc"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, COATED in 1 BOTTLE (67296-1834-1)", "package_ndc": "67296-1834-1", "marketing_start_date": "20210422"}, {"sample": false, "description": "20 TABLET, COATED in 1 BOTTLE (67296-1834-2)", "package_ndc": "67296-1834-2", "marketing_start_date": "20210422"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (67296-1834-3)", "package_ndc": "67296-1834-3", "marketing_start_date": "20210422"}, {"sample": false, "description": "40 TABLET, COATED in 1 BOTTLE (67296-1834-4)", "package_ndc": "67296-1834-4", "marketing_start_date": "20210422"}, {"sample": false, "description": "6 TABLET, COATED in 1 BOTTLE (67296-1834-6)", "package_ndc": "67296-1834-6", "marketing_start_date": "20210422"}, {"sample": false, "description": "15 TABLET, COATED in 1 BOTTLE (67296-1834-7)", "package_ndc": "67296-1834-7", "marketing_start_date": "20210422"}], "brand_name": "Tramadol Hydrochloride", "product_id": "67296-1834_4387f592-853f-01ea-e063-6394a90a6a4f", "dosage_form": "TABLET, COATED", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "67296-1834", "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": "ANDA208708", "marketing_category": "ANDA", "marketing_start_date": "20210422", "listing_expiration_date": "20261231"}