phentermine hydrochloride

Generic: phentermine hydrochloride

Labeler: kvk-tech, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name phentermine hydrochloride
Generic Name phentermine hydrochloride
Labeler kvk-tech, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

phentermine hydrochloride 37.5 mg/1

Manufacturer
KVK-TECH, Inc.

Identifiers & Regulatory

Product NDC 10702-025
Product ID 10702-025_1159ef2a-b2ca-518e-e063-6394a90a7543
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040876
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 10702025
Hyphenated Format 10702-025

Supplemental Identifiers

RxCUI
803348 803353
UNII
0K2I505OTV

Packaging Origin

Original Packager
true

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 ANDA040876 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 37.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (10702-025-01)
  • 30 TABLET in 1 BOTTLE (10702-025-03)
  • 1000 TABLET in 1 BOTTLE (10702-025-10)
source: ndc

Packages (3)

10702-025-01 100 TABLET in 1 BOTTLE (10702-025-01) 10702-025-03 30 TABLET in 1 BOTTLE (10702-025-03) 10702-025-10 1000 TABLET in 1 BOTTLE (10702-025-10)

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": "1159ef2a-b2ca-518e-e063-6394a90a7543", "openfda": {"unii": ["0K2I505OTV"], "rxcui": ["803348", "803353"], "spl_set_id": ["3b44d104-a7d0-4366-9d42-63f784f3cb22"], "manufacturer_name": ["KVK-TECH, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (10702-025-01)", "package_ndc": "10702-025-01", "marketing_start_date": "20120815"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (10702-025-03)", "package_ndc": "10702-025-03", "marketing_start_date": "20120815"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (10702-025-10)", "package_ndc": "10702-025-10", "marketing_start_date": "20120815"}], "brand_name": "Phentermine Hydrochloride", "product_id": "10702-025_1159ef2a-b2ca-518e-e063-6394a90a7543", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "10702-025", "dea_schedule": "CIV", "generic_name": "Phentermine Hydrochloride", "labeler_name": "KVK-TECH, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phentermine Hydrochloride", "active_ingredients": [{"name": "PHENTERMINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA040876", "marketing_category": "ANDA", "marketing_start_date": "20120815", "listing_expiration_date": "20261231"}