Phentermine Hydrochloride

Generic: Phentermine Hydrochloride

Labeler: Bryant Ranch Prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Active

Drug Facts

Product Profile

Brand Name Phentermine Hydrochloride
Generic Name Phentermine Hydrochloride
Labeler Bryant Ranch Prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

PHENTERMINE HYDROCHLORIDE 37.5 mg/1

Identifiers & Regulatory

Product NDC 63629-1044
Product ID 63629-1044_fbec1189-5c39-a0e8-e053-6394a90aa02f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200272
DEA Schedule CIV
Listing Expiration 2026-12-31
Marketing Start 2011-03-08

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 636291044
Hyphenated Format 63629-1044

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 ANDA200272 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 37.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (63629-1044-1)
source: ndc

Packages (1)

Ingredients (1)

PHENTERMINE HYDROCHLORIDE (37.5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fbec1189-5c39-a0e8-e053-6394a90aa02f", "openfda": {"unii": ["0K2I505OTV"], "rxcui": ["803353"], "spl_set_id": ["7e370e9c-b8ab-4313-85d6-2f3ccd22f7ff"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63629-1044-1)", "package_ndc": "63629-1044-1", "marketing_start_date": "20190701"}], "brand_name": "Phentermine Hydrochloride", "product_id": "63629-1044_fbec1189-5c39-a0e8-e053-6394a90aa02f", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "63629-1044", "dea_schedule": "CIV", "generic_name": "Phentermine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phentermine Hydrochloride", "active_ingredients": [{"name": "PHENTERMINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA200272", "marketing_category": "ANDA", "marketing_start_date": "20110308", "listing_expiration_date": "20261231"}