phentermine hydrochloride

Generic: phentermine hydrochloride

Labeler: elite laboratories, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name phentermine hydrochloride
Generic Name phentermine hydrochloride
Labeler elite laboratories, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

phentermine hydrochloride 37.5 mg/1

Manufacturer
Elite Laboratories, Inc.

Identifiers & Regulatory

Product NDC 64850-810
Product ID 64850-810_f2b9f70f-b5e3-4e6e-8607-5c73afbe9677
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040190
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2014-05-01

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 64850810
Hyphenated Format 64850-810

Supplemental Identifiers

RxCUI
803353
UPC
0364850810012 0364850810104
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 ANDA040190 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 37.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (64850-810-01)
  • 1000 TABLET in 1 BOTTLE (64850-810-10)
source: ndc

Packages (2)

64850-810-01 100 TABLET in 1 BOTTLE (64850-810-01) 64850-810-10 1000 TABLET in 1 BOTTLE (64850-810-10)

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": "f2b9f70f-b5e3-4e6e-8607-5c73afbe9677", "openfda": {"upc": ["0364850810012", "0364850810104"], "unii": ["0K2I505OTV"], "rxcui": ["803353"], "spl_set_id": ["0b7ad9c0-9e1e-4a69-802b-28f44267e34d"], "manufacturer_name": ["Elite Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (64850-810-01)", "package_ndc": "64850-810-01", "marketing_start_date": "20140501"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (64850-810-10)", "package_ndc": "64850-810-10", "marketing_start_date": "20140501"}], "brand_name": "Phentermine Hydrochloride", "product_id": "64850-810_f2b9f70f-b5e3-4e6e-8607-5c73afbe9677", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "64850-810", "dea_schedule": "CIV", "generic_name": "Phentermine Hydrochloride", "labeler_name": "Elite Laboratories, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phentermine Hydrochloride", "active_ingredients": [{"name": "PHENTERMINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA040190", "marketing_category": "ANDA", "marketing_start_date": "20140501", "listing_expiration_date": "20261231"}