tramadol hydrochloride
Generic: tramadol hydrochloride
Labeler: st. mary's medical park pharmacyDrug Facts
Product Profile
Brand Name
tramadol hydrochloride
Generic Name
tramadol hydrochloride
Labeler
st. mary's medical park pharmacy
Dosage Form
TABLET
Routes
Active Ingredients
tramadol hydrochloride 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
60760-727
Product ID
60760-727_4b9860c4-208c-30bc-e063-6294a90a5b71
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075968
DEA Schedule
civ
Listing Expiration
2027-12-31
Marketing Start
2024-08-05
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60760727
Hyphenated Format
60760-727
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
ANDA075968 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 9 TABLET in 1 BOTTLE, PLASTIC (60760-727-09)
- 20 TABLET in 1 BOTTLE, PLASTIC (60760-727-20)
- 30 TABLET in 1 BOTTLE, PLASTIC (60760-727-30)
- 50 TABLET in 1 BOTTLE, PLASTIC (60760-727-50)
- 60 TABLET in 1 BOTTLE, PLASTIC (60760-727-60)
- 90 TABLET in 1 BOTTLE, PLASTIC (60760-727-90)
- 120 TABLET in 1 BOTTLE, PLASTIC (60760-727-92)
- 180 TABLET in 1 BOTTLE, PLASTIC (60760-727-98)
Packages (8)
60760-727-09
9 TABLET in 1 BOTTLE, PLASTIC (60760-727-09)
60760-727-20
20 TABLET in 1 BOTTLE, PLASTIC (60760-727-20)
60760-727-30
30 TABLET in 1 BOTTLE, PLASTIC (60760-727-30)
60760-727-50
50 TABLET in 1 BOTTLE, PLASTIC (60760-727-50)
60760-727-60
60 TABLET in 1 BOTTLE, PLASTIC (60760-727-60)
60760-727-90
90 TABLET in 1 BOTTLE, PLASTIC (60760-727-90)
60760-727-92
120 TABLET in 1 BOTTLE, PLASTIC (60760-727-92)
60760-727-98
180 TABLET in 1 BOTTLE, PLASTIC (60760-727-98)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4b9860c4-208c-30bc-e063-6294a90a5b71", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["835603"], "spl_set_id": ["42de8c3a-0441-5d46-e063-6294a90a2079"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "9 TABLET in 1 BOTTLE, PLASTIC (60760-727-09)", "package_ndc": "60760-727-09", "marketing_start_date": "20260223"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (60760-727-20)", "package_ndc": "60760-727-20", "marketing_start_date": "20251113"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (60760-727-30)", "package_ndc": "60760-727-30", "marketing_start_date": "20251105"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE, PLASTIC (60760-727-50)", "package_ndc": "60760-727-50", "marketing_start_date": "20251105"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (60760-727-60)", "package_ndc": "60760-727-60", "marketing_start_date": "20251229"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (60760-727-90)", "package_ndc": "60760-727-90", "marketing_start_date": "20251105"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE, PLASTIC (60760-727-92)", "package_ndc": "60760-727-92", "marketing_start_date": "20260216"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE, PLASTIC (60760-727-98)", "package_ndc": "60760-727-98", "marketing_start_date": "20260216"}], "brand_name": "Tramadol Hydrochloride", "product_id": "60760-727_4b9860c4-208c-30bc-e063-6294a90a5b71", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "60760-727", "dea_schedule": "CIV", "generic_name": "Tramadol Hydrochloride", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tramadol Hydrochloride", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA075968", "marketing_category": "ANDA", "marketing_start_date": "20240805", "listing_expiration_date": "20271231"}