Phentermine Hydrochloride

Generic: Phentermine Hydrochloride

Labeler: TAGI Pharma, Inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive

Drug Facts

Product Profile

Brand Name Phentermine Hydrochloride
Generic Name Phentermine Hydrochloride
Labeler TAGI Pharma, Inc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

PHENTERMINE HYDROCHLORIDE 15 mg/1

Identifiers & Regulatory

Product NDC 51224-203
Product ID 51224-203_daad17fe-5fa7-4595-aff9-50b141a6aa31
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202248
DEA Schedule CIV
Marketing Start 2012-02-17
Marketing End 2026-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51224203
Hyphenated Format 51224-203

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 ANDA202248 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (51224-203-50)
  • 1000 CAPSULE in 1 BOTTLE (51224-203-70)
source: ndc

Packages (2)

Ingredients (1)

PHENTERMINE HYDROCHLORIDE (15 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "daad17fe-5fa7-4595-aff9-50b141a6aa31", "openfda": {"upc": ["0351224203709", "0351224203501", "0351224202504", "0351224202702"], "unii": ["0K2I505OTV"], "rxcui": ["900038", "968766"], "spl_set_id": ["2acb0c69-0089-4817-86ad-6df592c0356e"], "manufacturer_name": ["TAGI Pharma, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (51224-203-50)", "package_ndc": "51224-203-50", "marketing_end_date": "20260228", "marketing_start_date": "20120217"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (51224-203-70)", "package_ndc": "51224-203-70", "marketing_end_date": "20260228", "marketing_start_date": "20120217"}], "brand_name": "Phentermine Hydrochloride", "product_id": "51224-203_daad17fe-5fa7-4595-aff9-50b141a6aa31", "dosage_form": "CAPSULE", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "51224-203", "dea_schedule": "CIV", "generic_name": "Phentermine Hydrochloride", "labeler_name": "TAGI Pharma, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phentermine Hydrochloride", "active_ingredients": [{"name": "PHENTERMINE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA202248", "marketing_category": "ANDA", "marketing_end_date": "20260228", "marketing_start_date": "20120217"}