tramadol hydrochloride
Generic: tramadol hydrochloride
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
tramadol hydrochloride
Generic Name
tramadol hydrochloride
Labeler
proficient rx lp
Dosage Form
TABLET, COATED
Routes
Active Ingredients
tramadol hydrochloride 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
63187-063
Product ID
63187-063_59d339c1-6ad2-4407-ac41-74e5f4dda6e8
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076003
DEA Schedule
civ
Listing Expiration
2026-12-31
Marketing Start
2010-11-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63187063
Hyphenated Format
63187-063
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
ANDA076003 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 15 TABLET, COATED in 1 BOTTLE (63187-063-15)
- 20 TABLET, COATED in 1 BOTTLE (63187-063-20)
- 30 TABLET, COATED in 1 BOTTLE (63187-063-30)
- 40 TABLET, COATED in 1 BOTTLE (63187-063-40)
- 60 TABLET, COATED in 1 BOTTLE (63187-063-60)
- 240 TABLET, COATED in 1 BOTTLE (63187-063-64)
- 120 TABLET, COATED in 1 BOTTLE (63187-063-72)
- 180 TABLET, COATED in 1 BOTTLE (63187-063-78)
- 90 TABLET, COATED in 1 BOTTLE (63187-063-90)
Packages (9)
63187-063-15
15 TABLET, COATED in 1 BOTTLE (63187-063-15)
63187-063-20
20 TABLET, COATED in 1 BOTTLE (63187-063-20)
63187-063-30
30 TABLET, COATED in 1 BOTTLE (63187-063-30)
63187-063-40
40 TABLET, COATED in 1 BOTTLE (63187-063-40)
63187-063-60
60 TABLET, COATED in 1 BOTTLE (63187-063-60)
63187-063-64
240 TABLET, COATED in 1 BOTTLE (63187-063-64)
63187-063-72
120 TABLET, COATED in 1 BOTTLE (63187-063-72)
63187-063-78
180 TABLET, COATED in 1 BOTTLE (63187-063-78)
63187-063-90
90 TABLET, COATED in 1 BOTTLE (63187-063-90)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "59d339c1-6ad2-4407-ac41-74e5f4dda6e8", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["835603"], "spl_set_id": ["50f4b752-20af-4ebf-9408-e78f30d2a3cc"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, COATED in 1 BOTTLE (63187-063-15)", "package_ndc": "63187-063-15", "marketing_start_date": "20170801"}, {"sample": false, "description": "20 TABLET, COATED in 1 BOTTLE (63187-063-20)", "package_ndc": "63187-063-20", "marketing_start_date": "20161101"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (63187-063-30)", "package_ndc": "63187-063-30", "marketing_start_date": "20140501"}, {"sample": false, "description": "40 TABLET, COATED in 1 BOTTLE (63187-063-40)", "package_ndc": "63187-063-40", "marketing_start_date": "20140501"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (63187-063-60)", "package_ndc": "63187-063-60", "marketing_start_date": "20140501"}, {"sample": false, "description": "240 TABLET, COATED in 1 BOTTLE (63187-063-64)", "package_ndc": "63187-063-64", "marketing_start_date": "20140501"}, {"sample": false, "description": "120 TABLET, COATED in 1 BOTTLE (63187-063-72)", "package_ndc": "63187-063-72", "marketing_start_date": "20140501"}, {"sample": false, "description": "180 TABLET, COATED in 1 BOTTLE (63187-063-78)", "package_ndc": "63187-063-78", "marketing_start_date": "20140501"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (63187-063-90)", "package_ndc": "63187-063-90", "marketing_start_date": "20140501"}], "brand_name": "Tramadol Hydrochloride", "product_id": "63187-063_59d339c1-6ad2-4407-ac41-74e5f4dda6e8", "dosage_form": "TABLET, COATED", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "63187-063", "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": "50 mg/1"}], "application_number": "ANDA076003", "marketing_category": "ANDA", "marketing_start_date": "20101115", "listing_expiration_date": "20261231"}