phentermine

Generic: phentermine hydrochloride

Labeler: aurolife pharma, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name phentermine
Generic Name phentermine hydrochloride
Labeler aurolife pharma, llc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

phentermine hydrochloride 15 mg/1

Manufacturer
Aurolife Pharma, LLC

Identifiers & Regulatory

Product NDC 13107-105
Product ID 13107-105_53dd7857-41fb-4da1-88f7-5c68a509bfb0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204318
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2017-03-20

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 13107105
Hyphenated Format 13107-105

Supplemental Identifiers

RxCUI
900038 968766
UNII
0K2I505OTV

Packaging Origin

Original Packager
true

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 (source: ndc)
Generic Name phentermine hydrochloride (source: ndc)
Application Number ANDA204318 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (13107-105-01)
  • 30 CAPSULE in 1 BOTTLE (13107-105-30)
source: ndc

Packages (2)

13107-105-01 100 CAPSULE in 1 BOTTLE (13107-105-01) 13107-105-30 30 CAPSULE in 1 BOTTLE (13107-105-30)

Ingredients (1)

phentermine hydrochloride (15 mg/1)

Linked Drug Pages (1)

Phentermine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "53dd7857-41fb-4da1-88f7-5c68a509bfb0", "openfda": {"unii": ["0K2I505OTV"], "rxcui": ["900038", "968766"], "spl_set_id": ["737eef3b-9a6b-4ab3-a25c-49d84d2a0197"], "manufacturer_name": ["Aurolife Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (13107-105-01)", "package_ndc": "13107-105-01", "marketing_start_date": "20170320"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (13107-105-30)", "package_ndc": "13107-105-30", "marketing_start_date": "20170320"}], "brand_name": "Phentermine", "product_id": "13107-105_53dd7857-41fb-4da1-88f7-5c68a509bfb0", "dosage_form": "CAPSULE", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "13107-105", "dea_schedule": "CIV", "generic_name": "Phentermine Hydrochloride", "labeler_name": "Aurolife Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phentermine", "active_ingredients": [{"name": "PHENTERMINE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA204318", "marketing_category": "ANDA", "marketing_start_date": "20170320", "listing_expiration_date": "20261231"}