phentermine hydrochloride

Generic: phentermine hydrochloride

Labeler: calvin scott & co., inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name phentermine hydrochloride
Generic Name phentermine hydrochloride
Labeler calvin scott & co., inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

phentermine hydrochloride 37.5 mg/1

Manufacturer
Calvin Scott & Co., Inc.

Identifiers & Regulatory

Product NDC 17224-904
Product ID 17224-904_f6e232c2-4182-6274-e053-6294a90a5e38
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205008
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2017-01-24

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 17224904
Hyphenated Format 17224-904

Supplemental Identifiers

RxCUI
803353
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 ANDA205008 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 37.5 mg/1
source: ndc
Packaging
  • 7 TABLET in 1 BOTTLE (17224-904-07)
  • 28 TABLET in 1 BOTTLE (17224-904-28)
  • 30 TABLET in 1 BOTTLE (17224-904-30)
  • 60 TABLET in 1 BOTTLE (17224-904-60)
source: ndc

Packages (4)

17224-904-07 7 TABLET in 1 BOTTLE (17224-904-07) 17224-904-28 28 TABLET in 1 BOTTLE (17224-904-28) 17224-904-30 30 TABLET in 1 BOTTLE (17224-904-30) 17224-904-60 60 TABLET in 1 BOTTLE (17224-904-60)

Ingredients (1)

phentermine hydrochloride (37.5 mg/1)

Linked Drug Pages (1)

Phentermine hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f6e232c2-4182-6274-e053-6294a90a5e38", "openfda": {"unii": ["0K2I505OTV"], "rxcui": ["803353"], "spl_set_id": ["3d1d4dde-1c7f-4a20-b8f8-897b1b284f80"], "manufacturer_name": ["Calvin Scott & Co., Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "7 TABLET in 1 BOTTLE (17224-904-07)", "package_ndc": "17224-904-07", "marketing_start_date": "20170124"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (17224-904-28)", "package_ndc": "17224-904-28", "marketing_start_date": "20170124"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (17224-904-30)", "package_ndc": "17224-904-30", "marketing_start_date": "20170124"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (17224-904-60)", "package_ndc": "17224-904-60", "marketing_start_date": "20170124"}], "brand_name": "Phentermine hydrochloride", "product_id": "17224-904_f6e232c2-4182-6274-e053-6294a90a5e38", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "17224-904", "dea_schedule": "CIV", "generic_name": "PHENTERMINE HYDROCHLORIDE", "labeler_name": "Calvin Scott & Co., Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phentermine hydrochloride", "active_ingredients": [{"name": "PHENTERMINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA205008", "marketing_category": "ANDA", "marketing_start_date": "20170124", "listing_expiration_date": "20261231"}