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 CAPSULE
Routes
ORAL
Active Ingredients

phentermine hydrochloride 30 mg/1

Manufacturer
Calvin Scott & Co., Inc.

Identifiers & Regulatory

Product NDC 17224-870
Product ID 17224-870_f8aba3a2-7dc5-fb9a-e053-6294a90ad49e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040886
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2012-08-07

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 17224870
Hyphenated Format 17224-870

Supplemental Identifiers

RxCUI
900038
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 ANDA040886 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 21 CAPSULE in 1 BOTTLE (17224-870-21)
  • 28 CAPSULE in 1 BOTTLE (17224-870-28)
  • 30 CAPSULE in 1 BOTTLE (17224-870-30)
  • 42 CAPSULE in 1 BOTTLE (17224-870-42)
source: ndc

Packages (4)

Ingredients (1)

phentermine hydrochloride (30 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f8aba3a2-7dc5-fb9a-e053-6294a90ad49e", "openfda": {"unii": ["0K2I505OTV"], "rxcui": ["900038"], "spl_set_id": ["2f3b738f-d66b-40c1-8e69-bcd50bce3e47"], "manufacturer_name": ["Calvin Scott & Co., Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "21 CAPSULE in 1 BOTTLE (17224-870-21)", "package_ndc": "17224-870-21", "marketing_start_date": "20120807"}, {"sample": false, "description": "28 CAPSULE in 1 BOTTLE (17224-870-28)", "package_ndc": "17224-870-28", "marketing_start_date": "20120807"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (17224-870-30)", "package_ndc": "17224-870-30", "marketing_start_date": "20120807"}, {"sample": false, "description": "42 CAPSULE in 1 BOTTLE (17224-870-42)", "package_ndc": "17224-870-42", "marketing_start_date": "20120807"}], "brand_name": "Phentermine Hydrochloride", "product_id": "17224-870_f8aba3a2-7dc5-fb9a-e053-6294a90ad49e", "dosage_form": "CAPSULE", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "17224-870", "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": "30 mg/1"}], "application_number": "ANDA040886", "marketing_category": "ANDA", "marketing_start_date": "20120807", "listing_expiration_date": "20261231"}