phentermine hydrochloride

Generic: phentermine hydrochloride

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name phentermine hydrochloride
Generic Name phentermine hydrochloride
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

phentermine hydrochloride 37.5 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-433
Product ID 72789-433_47f6fb4d-1048-74df-e063-6394a90a5fa9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200272
DEA Schedule civ
Marketing Start 2024-02-15
Marketing End 2028-04-30

Pharmacologic Class

Classes
appetite suppression [pe] increased sympathetic activity [pe] sympathomimetic amine anorectic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72789433
Hyphenated Format 72789-433

Supplemental Identifiers

RxCUI
803353
UPC
0372789433158
UNII
0K2I505OTV

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 phentermine hydrochloride (source: ndc)
Generic Name phentermine hydrochloride (source: ndc)
Application Number ANDA200272 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 37.5 mg/1
source: ndc
Packaging
  • 7 TABLET in 1 BOTTLE, PLASTIC (72789-433-07)
  • 14 TABLET in 1 BOTTLE, PLASTIC (72789-433-14)
  • 15 TABLET in 1 BOTTLE, PLASTIC (72789-433-15)
  • 28 TABLET in 1 BOTTLE, PLASTIC (72789-433-28)
  • 30 TABLET in 1 BOTTLE, PLASTIC (72789-433-30)
  • 45 TABLET in 1 BOTTLE, PLASTIC (72789-433-45)
  • 60 TABLET in 1 BOTTLE, PLASTIC (72789-433-60)
  • 90 TABLET in 1 BOTTLE, PLASTIC (72789-433-90)
source: ndc

Packages (8)

Ingredients (1)

phentermine hydrochloride (37.5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47f6fb4d-1048-74df-e063-6394a90a5fa9", "openfda": {"upc": ["0372789433158"], "unii": ["0K2I505OTV"], "rxcui": ["803353"], "spl_set_id": ["19f1ce79-65f4-4bf4-a9ff-6ca0a131530f"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "7 TABLET in 1 BOTTLE, PLASTIC (72789-433-07)", "package_ndc": "72789-433-07", "marketing_end_date": "20280430", "marketing_start_date": "20241024"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE, PLASTIC (72789-433-14)", "package_ndc": "72789-433-14", "marketing_end_date": "20280430", "marketing_start_date": "20250721"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE, PLASTIC (72789-433-15)", "package_ndc": "72789-433-15", "marketing_end_date": "20280430", "marketing_start_date": "20241001"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE, PLASTIC (72789-433-28)", "package_ndc": "72789-433-28", "marketing_end_date": "20280430", "marketing_start_date": "20241104"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-433-30)", "package_ndc": "72789-433-30", "marketing_end_date": "20280430", "marketing_start_date": "20241106"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE, PLASTIC (72789-433-45)", "package_ndc": "72789-433-45", "marketing_end_date": "20280430", "marketing_start_date": "20241107"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (72789-433-60)", "package_ndc": "72789-433-60", "marketing_end_date": "20280430", "marketing_start_date": "20241018"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-433-90)", "package_ndc": "72789-433-90", "marketing_end_date": "20280430", "marketing_start_date": "20241018"}], "brand_name": "Phentermine Hydrochloride", "product_id": "72789-433_47f6fb4d-1048-74df-e063-6394a90a5fa9", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "72789-433", "dea_schedule": "CIV", "generic_name": "Phentermine Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phentermine Hydrochloride", "active_ingredients": [{"name": "PHENTERMINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA200272", "marketing_category": "ANDA", "marketing_end_date": "20280430", "marketing_start_date": "20240215"}