phendimetrazine tartrate
Generic: phendimetrazine tartrate
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
phendimetrazine tartrate
Generic Name
phendimetrazine tartrate
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
phendimetrazine tartrate 35 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-6552
Product ID
50090-6552_a420ce0d-e458-46ca-aa9c-aaba680e455b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA091042
DEA Schedule
ciii
Listing Expiration
2026-12-31
Marketing Start
2010-09-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500906552
Hyphenated Format
50090-6552
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
phendimetrazine tartrate (source: ndc)
Generic Name
phendimetrazine tartrate (source: ndc)
Application Number
ANDA091042 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 35 mg/1
Packaging
- 90 TABLET in 1 BOTTLE (50090-6552-2)
- 30 TABLET in 1 BOTTLE (50090-6552-9)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a420ce0d-e458-46ca-aa9c-aaba680e455b", "openfda": {"unii": ["6985IP0T80"], "rxcui": ["979549"], "spl_set_id": ["7adaf128-fef4-4bbf-8b4a-875fe46bf68a"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6552-2)", "package_ndc": "50090-6552-2", "marketing_start_date": "20230712"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-6552-9)", "package_ndc": "50090-6552-9", "marketing_start_date": "20230712"}], "brand_name": "Phendimetrazine Tartrate", "product_id": "50090-6552_a420ce0d-e458-46ca-aa9c-aaba680e455b", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "50090-6552", "dea_schedule": "CIII", "generic_name": "Phendimetrazine Tartrate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phendimetrazine Tartrate", "active_ingredients": [{"name": "PHENDIMETRAZINE TARTRATE", "strength": "35 mg/1"}], "application_number": "ANDA091042", "marketing_category": "ANDA", "marketing_start_date": "20100915", "listing_expiration_date": "20261231"}