phentermine hydrochloride

Generic: phentermine hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name phentermine hydrochloride
Generic Name phentermine hydrochloride
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

phentermine hydrochloride 30 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-1498
Product ID 50090-1498_9b3a977c-5275-47b5-87ff-1660783e7a9a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040526
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2013-08-12

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 500901498
Hyphenated Format 50090-1498

Supplemental Identifiers

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 ANDA040526 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-1498-0)
  • 14 TABLET in 1 BOTTLE (50090-1498-1)
  • 7 TABLET in 1 BOTTLE (50090-1498-2)
  • 60 TABLET in 1 BOTTLE (50090-1498-3)
  • 45 TABLET in 1 BOTTLE (50090-1498-4)
  • 28 TABLET in 1 BOTTLE (50090-1498-8)
source: ndc

Packages (6)

50090-1498-0 30 TABLET in 1 BOTTLE (50090-1498-0) 50090-1498-1 14 TABLET in 1 BOTTLE (50090-1498-1) 50090-1498-2 7 TABLET in 1 BOTTLE (50090-1498-2) 50090-1498-3 60 TABLET in 1 BOTTLE (50090-1498-3) 50090-1498-4 45 TABLET in 1 BOTTLE (50090-1498-4) 50090-1498-8 28 TABLET in 1 BOTTLE (50090-1498-8)

Ingredients (1)

phentermine hydrochloride (30 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": "9b3a977c-5275-47b5-87ff-1660783e7a9a", "openfda": {"unii": ["0K2I505OTV"], "spl_set_id": ["0e893b62-bb07-4984-9f0a-3601435fbc27"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-1498-0)", "package_ndc": "50090-1498-0", "marketing_start_date": "20141205"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (50090-1498-1)", "package_ndc": "50090-1498-1", "marketing_start_date": "20141205"}, {"sample": false, "description": "7 TABLET in 1 BOTTLE (50090-1498-2)", "package_ndc": "50090-1498-2", "marketing_start_date": "20141205"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-1498-3)", "package_ndc": "50090-1498-3", "marketing_start_date": "20141205"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE (50090-1498-4)", "package_ndc": "50090-1498-4", "marketing_start_date": "20141205"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (50090-1498-8)", "package_ndc": "50090-1498-8", "marketing_start_date": "20141205"}], "brand_name": "Phentermine Hydrochloride", "product_id": "50090-1498_9b3a977c-5275-47b5-87ff-1660783e7a9a", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "50090-1498", "dea_schedule": "CIV", "generic_name": "Phentermine Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phentermine Hydrochloride", "active_ingredients": [{"name": "PHENTERMINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA040526", "marketing_category": "ANDA", "marketing_start_date": "20130812", "listing_expiration_date": "20261231"}