phentermine

Generic: phentermine hydrochloride

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

Drug Facts

Product Profile

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

phentermine hydrochloride 37.5 mg/1

Manufacturer
Calvin Scott & Co., Inc.

Identifiers & Regulatory

Product NDC 17224-890
Product ID 17224-890_3389935b-316a-971a-e063-6394a90abaff
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040887
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2012-08-15

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 17224890
Hyphenated Format 17224-890

Supplemental Identifiers

RxCUI
803348
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 (source: ndc)
Generic Name phentermine hydrochloride (source: ndc)
Application Number ANDA040887 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 37.5 mg/1
source: ndc
Packaging
  • 14 CAPSULE in 1 BOTTLE (17224-890-14)
  • 21 CAPSULE in 1 BOTTLE (17224-890-21)
  • 28 CAPSULE in 1 BOTTLE (17224-890-28)
  • 30 CAPSULE in 1 BOTTLE (17224-890-30)
  • 56 CAPSULE in 1 BOTTLE (17224-890-56)
source: ndc

Packages (5)

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": "3389935b-316a-971a-e063-6394a90abaff", "openfda": {"unii": ["0K2I505OTV"], "rxcui": ["803348"], "spl_set_id": ["27e88ebe-6247-4598-8ef2-c882992ed579"], "manufacturer_name": ["Calvin Scott & Co., Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "14 CAPSULE in 1 BOTTLE (17224-890-14)", "package_ndc": "17224-890-14", "marketing_start_date": "20120815"}, {"sample": false, "description": "21 CAPSULE in 1 BOTTLE (17224-890-21)", "package_ndc": "17224-890-21", "marketing_start_date": "20120815"}, {"sample": false, "description": "28 CAPSULE in 1 BOTTLE (17224-890-28)", "package_ndc": "17224-890-28", "marketing_start_date": "20120815"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (17224-890-30)", "package_ndc": "17224-890-30", "marketing_start_date": "20120815"}, {"sample": false, "description": "56 CAPSULE in 1 BOTTLE (17224-890-56)", "package_ndc": "17224-890-56", "marketing_start_date": "20120815"}], "brand_name": "Phentermine", "product_id": "17224-890_3389935b-316a-971a-e063-6394a90abaff", "dosage_form": "CAPSULE", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "17224-890", "dea_schedule": "CIV", "generic_name": "PHENTERMINE HYDROCHLORIDE", "labeler_name": "Calvin Scott & Co., Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phentermine", "active_ingredients": [{"name": "PHENTERMINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA040887", "marketing_category": "ANDA", "marketing_start_date": "20120815", "listing_expiration_date": "20261231"}