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 37.5 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-1679
Product ID 50090-1679_a471924e-e01a-4665-9ba1-1eaea935a7ad
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040876
DEA Schedule civ
Listing Expiration 2027-12-31
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 500901679
Hyphenated Format 50090-1679

Supplemental Identifiers

RxCUI
803353
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
  • 30 TABLET in 1 BOTTLE (50090-1679-0)
  • 45 TABLET in 1 BOTTLE (50090-1679-1)
  • 60 TABLET in 1 BOTTLE (50090-1679-2)
  • 28 TABLET in 1 BOTTLE (50090-1679-3)
  • 7 TABLET in 1 BOTTLE (50090-1679-4)
  • 14 TABLET in 1 BOTTLE (50090-1679-5)
  • 90 TABLET in 1 BOTTLE (50090-1679-6)
source: ndc

Packages (7)

50090-1679-0 30 TABLET in 1 BOTTLE (50090-1679-0) 50090-1679-1 45 TABLET in 1 BOTTLE (50090-1679-1) 50090-1679-2 60 TABLET in 1 BOTTLE (50090-1679-2) 50090-1679-3 28 TABLET in 1 BOTTLE (50090-1679-3) 50090-1679-4 7 TABLET in 1 BOTTLE (50090-1679-4) 50090-1679-5 14 TABLET in 1 BOTTLE (50090-1679-5) 50090-1679-6 90 TABLET in 1 BOTTLE (50090-1679-6)

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": "a471924e-e01a-4665-9ba1-1eaea935a7ad", "openfda": {"unii": ["0K2I505OTV"], "rxcui": ["803353"], "spl_set_id": ["86ec6b9d-2934-4bad-8a80-0b60e2f912f3"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-1679-0)", "package_ndc": "50090-1679-0", "marketing_start_date": "20150203"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE (50090-1679-1)", "package_ndc": "50090-1679-1", "marketing_start_date": "20150203"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-1679-2)", "package_ndc": "50090-1679-2", "marketing_start_date": "20150203"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (50090-1679-3)", "package_ndc": "50090-1679-3", "marketing_start_date": "20150428"}, {"sample": false, "description": "7 TABLET in 1 BOTTLE (50090-1679-4)", "package_ndc": "50090-1679-4", "marketing_start_date": "20150428"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (50090-1679-5)", "package_ndc": "50090-1679-5", "marketing_start_date": "20150428"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-1679-6)", "package_ndc": "50090-1679-6", "marketing_start_date": "20180806"}], "brand_name": "Phentermine Hydrochloride", "product_id": "50090-1679_a471924e-e01a-4665-9ba1-1eaea935a7ad", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "50090-1679", "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": "37.5 mg/1"}], "application_number": "ANDA040876", "marketing_category": "ANDA", "marketing_start_date": "20120815", "listing_expiration_date": "20271231"}