phendimetrazine tartrate
Generic: phendimetrazine tartrate
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
phendimetrazine tartrate
Generic Name
phendimetrazine tartrate
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
TABLET
Routes
Active Ingredients
phendimetrazine tartrate 35 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
43063-510
Product ID
43063-510_2b33c59d-56f9-8ed2-e063-6394a90a1ad6
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
43063510
Hyphenated Format
43063-510
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
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
- 7 TABLET in 1 BOTTLE, PLASTIC (43063-510-07)
- 14 TABLET in 1 BOTTLE, PLASTIC (43063-510-14)
- 28 TABLET in 1 BOTTLE, PLASTIC (43063-510-28)
- 30 TABLET in 1 BOTTLE, PLASTIC (43063-510-30)
- 42 TABLET in 1 BOTTLE, PLASTIC (43063-510-42)
- 56 TABLET in 1 BOTTLE, PLASTIC (43063-510-56)
- 60 TABLET in 1 BOTTLE, PLASTIC (43063-510-60)
- 135 TABLET in 1 BOTTLE, PLASTIC (43063-510-81)
- 112 TABLET in 1 BOTTLE, PLASTIC (43063-510-88)
- 90 TABLET in 1 BOTTLE, PLASTIC (43063-510-90)
Packages (10)
43063-510-07
7 TABLET in 1 BOTTLE, PLASTIC (43063-510-07)
43063-510-14
14 TABLET in 1 BOTTLE, PLASTIC (43063-510-14)
43063-510-28
28 TABLET in 1 BOTTLE, PLASTIC (43063-510-28)
43063-510-30
30 TABLET in 1 BOTTLE, PLASTIC (43063-510-30)
43063-510-42
42 TABLET in 1 BOTTLE, PLASTIC (43063-510-42)
43063-510-56
56 TABLET in 1 BOTTLE, PLASTIC (43063-510-56)
43063-510-60
60 TABLET in 1 BOTTLE, PLASTIC (43063-510-60)
43063-510-81
135 TABLET in 1 BOTTLE, PLASTIC (43063-510-81)
43063-510-88
112 TABLET in 1 BOTTLE, PLASTIC (43063-510-88)
43063-510-90
90 TABLET in 1 BOTTLE, PLASTIC (43063-510-90)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b33c59d-56f9-8ed2-e063-6394a90a1ad6", "openfda": {"upc": ["0343063510568"], "unii": ["6985IP0T80"], "rxcui": ["979549"], "spl_set_id": ["467ae7d7-e342-423b-be89-5d38c1abf3c9"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "7 TABLET in 1 BOTTLE, PLASTIC (43063-510-07)", "package_ndc": "43063-510-07", "marketing_start_date": "20170623"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE, PLASTIC (43063-510-14)", "package_ndc": "43063-510-14", "marketing_start_date": "20170411"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE, PLASTIC (43063-510-28)", "package_ndc": "43063-510-28", "marketing_start_date": "20100915"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-510-30)", "package_ndc": "43063-510-30", "marketing_start_date": "20100915"}, {"sample": false, "description": "42 TABLET in 1 BOTTLE, PLASTIC (43063-510-42)", "package_ndc": "43063-510-42", "marketing_start_date": "20231006"}, {"sample": false, "description": "56 TABLET in 1 BOTTLE, PLASTIC (43063-510-56)", "package_ndc": "43063-510-56", "marketing_start_date": "20170623"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (43063-510-60)", "package_ndc": "43063-510-60", "marketing_start_date": "20100915"}, {"sample": false, "description": "135 TABLET in 1 BOTTLE, PLASTIC (43063-510-81)", "package_ndc": "43063-510-81", "marketing_start_date": "20180501"}, {"sample": false, "description": "112 TABLET in 1 BOTTLE, PLASTIC (43063-510-88)", "package_ndc": "43063-510-88", "marketing_start_date": "20170419"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (43063-510-90)", "package_ndc": "43063-510-90", "marketing_start_date": "20170419"}], "brand_name": "Phendimetrazine Tartrate", "product_id": "43063-510_2b33c59d-56f9-8ed2-e063-6394a90a1ad6", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "43063-510", "dea_schedule": "CIII", "generic_name": "Phendimetrazine Tartrate", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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"}