phentermine hydrochloride

Generic: phentermine hydrochloride

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

Drug Facts

Product Profile

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

phentermine hydrochloride 37.5 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-3819
Product ID 68071-3819_315baaa6-5129-f27b-e063-6294a90a2c91
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 680713819
Hyphenated Format 68071-3819

Supplemental Identifiers

RxCUI
803353
UPC
0368071381917
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 ANDA040876 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 37.5 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (68071-3819-1)
source: ndc

Packages (1)

68071-3819-1 1000 TABLET in 1 BOTTLE (68071-3819-1)

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": "315baaa6-5129-f27b-e063-6294a90a2c91", "openfda": {"upc": ["0368071381917"], "unii": ["0K2I505OTV"], "rxcui": ["803353"], "spl_set_id": ["315b8a94-b7cc-1b47-e063-6294a90a2d39"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (68071-3819-1)", "package_ndc": "68071-3819-1", "marketing_start_date": "20250327"}], "brand_name": "Phentermine Hydrochloride", "product_id": "68071-3819_315baaa6-5129-f27b-e063-6294a90a2c91", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "68071-3819", "dea_schedule": "CIV", "generic_name": "Phentermine Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,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"}