phentermine hydrochloride

Generic: phentermine hydrochloride

Labeler: chartwell rx, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name phentermine hydrochloride
Generic Name phentermine hydrochloride
Labeler chartwell rx, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

phentermine hydrochloride 8 mg/1

Manufacturer
Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-959
Product ID 62135-959_3cbb33bd-89d0-952d-e063-6294a90a4d79
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA083923
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 1976-07-01

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 62135959
Hyphenated Format 62135-959

Supplemental Identifiers

RxCUI
826919
UPC
0362135959906
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 ANDA083923 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 8 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (62135-959-90)
source: ndc

Packages (1)

62135-959-90 90 TABLET in 1 BOTTLE (62135-959-90)

Ingredients (1)

phentermine hydrochloride (8 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": "3cbb33bd-89d0-952d-e063-6294a90a4d79", "openfda": {"upc": ["0362135959906"], "unii": ["0K2I505OTV"], "rxcui": ["826919"], "spl_set_id": ["d70f0be3-fcc7-4a1d-9a82-bb1bb21a1528"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (62135-959-90)", "package_ndc": "62135-959-90", "marketing_start_date": "20250724"}], "brand_name": "Phentermine Hydrochloride", "product_id": "62135-959_3cbb33bd-89d0-952d-e063-6294a90a4d79", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "62135-959", "dea_schedule": "CIV", "generic_name": "Phentermine Hydrochloride", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phentermine Hydrochloride", "active_ingredients": [{"name": "PHENTERMINE HYDROCHLORIDE", "strength": "8 mg/1"}], "application_number": "ANDA083923", "marketing_category": "ANDA", "marketing_start_date": "19760701", "listing_expiration_date": "20261231"}