phentermine hydrochloride

Generic: phentermine hydrochloride

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name phentermine hydrochloride
Generic Name phentermine hydrochloride
Labeler pd-rx pharmaceuticals, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

phentermine hydrochloride 37.5 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-182
Product ID 43063-182_41377de9-db46-c1f1-e063-6394a90a6a48
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040887
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 43063182
Hyphenated Format 43063-182

Supplemental Identifiers

RxCUI
803348
UPC
0343063182307
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 ANDA040887 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 37.5 mg/1
source: ndc
Packaging
  • 15 CAPSULE in 1 BOTTLE, PLASTIC (43063-182-15)
  • 30 CAPSULE in 1 BOTTLE, PLASTIC (43063-182-30)
  • 60 CAPSULE in 1 BOTTLE, PLASTIC (43063-182-60)
source: ndc

Packages (3)

43063-182-15 15 CAPSULE in 1 BOTTLE, PLASTIC (43063-182-15) 43063-182-30 30 CAPSULE in 1 BOTTLE, PLASTIC (43063-182-30) 43063-182-60 60 CAPSULE in 1 BOTTLE, PLASTIC (43063-182-60)

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": "41377de9-db46-c1f1-e063-6394a90a6a48", "openfda": {"upc": ["0343063182307"], "unii": ["0K2I505OTV"], "rxcui": ["803348"], "spl_set_id": ["378d863a-6977-4543-ae50-c3684a6abd9b"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "15 CAPSULE in 1 BOTTLE, PLASTIC (43063-182-15)", "package_ndc": "43063-182-15", "marketing_start_date": "20120831"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (43063-182-30)", "package_ndc": "43063-182-30", "marketing_start_date": "20120831"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE, PLASTIC (43063-182-60)", "package_ndc": "43063-182-60", "marketing_start_date": "20120831"}], "brand_name": "Phentermine Hydrochloride", "product_id": "43063-182_41377de9-db46-c1f1-e063-6394a90a6a48", "dosage_form": "CAPSULE", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "43063-182", "dea_schedule": "CIV", "generic_name": "Phentermine Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phentermine Hydrochloride", "active_ingredients": [{"name": "PHENTERMINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA040887", "marketing_category": "ANDA", "marketing_start_date": "20120815", "listing_expiration_date": "20261231"}