phentermine hydrochloride

Generic: phentermine hydrochloride

Labeler: sunrise pharmaceutical, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name phentermine hydrochloride
Generic Name phentermine hydrochloride
Labeler sunrise pharmaceutical, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

phentermine hydrochloride 37.5 mg/1

Manufacturer
SUNRISE PHARMACEUTICAL, INC.

Identifiers & Regulatory

Product NDC 11534-160
Product ID 11534-160_a9fd0c08-60ae-4015-85c7-803989d00745
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205008
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2017-01-24

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 11534160
Hyphenated Format 11534-160

Supplemental Identifiers

RxCUI
803348 803353
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 hydrochloride (source: ndc)
Generic Name phentermine hydrochloride (source: ndc)
Application Number ANDA205008 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 37.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (11534-160-01)
  • 1000 TABLET in 1 BOTTLE (11534-160-03)
  • 30 TABLET in 1 BOTTLE (11534-160-30)
source: ndc

Packages (3)

11534-160-01 100 TABLET in 1 BOTTLE (11534-160-01) 11534-160-03 1000 TABLET in 1 BOTTLE (11534-160-03) 11534-160-30 30 TABLET in 1 BOTTLE (11534-160-30)

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": "a9fd0c08-60ae-4015-85c7-803989d00745", "openfda": {"unii": ["0K2I505OTV"], "rxcui": ["803348", "803353"], "spl_set_id": ["43024f64-2d77-49a9-80fd-ad07a86c69a3"], "manufacturer_name": ["SUNRISE PHARMACEUTICAL, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (11534-160-01)", "package_ndc": "11534-160-01", "marketing_start_date": "20170124"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (11534-160-03)", "package_ndc": "11534-160-03", "marketing_start_date": "20170124"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (11534-160-30)", "package_ndc": "11534-160-30", "marketing_start_date": "20170124"}], "brand_name": "Phentermine hydrochloride", "product_id": "11534-160_a9fd0c08-60ae-4015-85c7-803989d00745", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "11534-160", "dea_schedule": "CIV", "generic_name": "phentermine hydrochloride", "labeler_name": "SUNRISE PHARMACEUTICAL, INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phentermine hydrochloride", "active_ingredients": [{"name": "PHENTERMINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA205008", "marketing_category": "ANDA", "marketing_start_date": "20170124", "listing_expiration_date": "20261231"}