phentermine hydrochloride

Generic: phentermine hydrochloride

Labeler: preferred pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name phentermine hydrochloride
Generic Name phentermine hydrochloride
Labeler preferred pharmaceuticals, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

phentermine hydrochloride 15 mg/1

Manufacturer
Preferred Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68788-7740
Product ID 68788-7740_d91aaa18-40c1-4a97-bf23-123f91e391d3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205019
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2020-07-01

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 687887740
Hyphenated Format 68788-7740

Supplemental Identifiers

RxCUI
968766
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 ANDA205019 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/1
source: ndc
Packaging
  • 7 CAPSULE in 1 BOTTLE (68788-7740-1)
  • 30 CAPSULE in 1 BOTTLE (68788-7740-3)
source: ndc

Packages (2)

68788-7740-1 7 CAPSULE in 1 BOTTLE (68788-7740-1) 68788-7740-3 30 CAPSULE in 1 BOTTLE (68788-7740-3)

Ingredients (1)

phentermine hydrochloride (15 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": "d91aaa18-40c1-4a97-bf23-123f91e391d3", "openfda": {"unii": ["0K2I505OTV"], "rxcui": ["968766"], "spl_set_id": ["70bc6f36-8087-4ccd-a396-a911c0ebae79"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "7 CAPSULE in 1 BOTTLE (68788-7740-1)", "package_ndc": "68788-7740-1", "marketing_start_date": "20200701"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (68788-7740-3)", "package_ndc": "68788-7740-3", "marketing_start_date": "20200701"}], "brand_name": "Phentermine Hydrochloride", "product_id": "68788-7740_d91aaa18-40c1-4a97-bf23-123f91e391d3", "dosage_form": "CAPSULE", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "68788-7740", "dea_schedule": "CIV", "generic_name": "phentermine hydrochloride", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phentermine Hydrochloride", "active_ingredients": [{"name": "PHENTERMINE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA205019", "marketing_category": "ANDA", "marketing_start_date": "20200701", "listing_expiration_date": "20261231"}