phentermine hydrochloride
Generic: phentermine hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
phentermine hydrochloride
Generic Name
phentermine hydrochloride
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
phentermine hydrochloride 37.5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-2488
Product ID
71335-2488_302f8c11-5717-4e3d-a5b2-41794d50c9d1
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA200272
DEA Schedule
civ
Listing Expiration
2026-12-31
Marketing Start
2024-02-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713352488
Hyphenated Format
71335-2488
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 37.5 mg/1
Packaging
- 90 TABLET in 1 BOTTLE (71335-2488-0)
- 30 TABLET in 1 BOTTLE (71335-2488-1)
- 15 TABLET in 1 BOTTLE (71335-2488-2)
- 28 TABLET in 1 BOTTLE (71335-2488-3)
- 7 TABLET in 1 BOTTLE (71335-2488-4)
- 14 TABLET in 1 BOTTLE (71335-2488-5)
- 60 TABLET in 1 BOTTLE (71335-2488-6)
- 45 TABLET in 1 BOTTLE (71335-2488-7)
- 2 TABLET in 1 BOTTLE (71335-2488-8)
- 21 TABLET in 1 BOTTLE (71335-2488-9)
Packages (10)
71335-2488-0
90 TABLET in 1 BOTTLE (71335-2488-0)
71335-2488-1
30 TABLET in 1 BOTTLE (71335-2488-1)
71335-2488-2
15 TABLET in 1 BOTTLE (71335-2488-2)
71335-2488-3
28 TABLET in 1 BOTTLE (71335-2488-3)
71335-2488-4
7 TABLET in 1 BOTTLE (71335-2488-4)
71335-2488-5
14 TABLET in 1 BOTTLE (71335-2488-5)
71335-2488-6
60 TABLET in 1 BOTTLE (71335-2488-6)
71335-2488-7
45 TABLET in 1 BOTTLE (71335-2488-7)
71335-2488-8
2 TABLET in 1 BOTTLE (71335-2488-8)
71335-2488-9
21 TABLET in 1 BOTTLE (71335-2488-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "302f8c11-5717-4e3d-a5b2-41794d50c9d1", "openfda": {"unii": ["0K2I505OTV"], "rxcui": ["803353"], "spl_set_id": ["e6939fcf-3db2-492a-99ed-a384cdeea7a2"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2488-0)", "package_ndc": "71335-2488-0", "marketing_start_date": "20240918"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2488-1)", "package_ndc": "71335-2488-1", "marketing_start_date": "20240918"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (71335-2488-2)", "package_ndc": "71335-2488-2", "marketing_start_date": "20240918"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-2488-3)", "package_ndc": "71335-2488-3", "marketing_start_date": "20240918"}, {"sample": false, "description": "7 TABLET in 1 BOTTLE (71335-2488-4)", "package_ndc": "71335-2488-4", "marketing_start_date": "20240918"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (71335-2488-5)", "package_ndc": "71335-2488-5", "marketing_start_date": "20240918"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-2488-6)", "package_ndc": "71335-2488-6", "marketing_start_date": "20240918"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE (71335-2488-7)", "package_ndc": "71335-2488-7", "marketing_start_date": "20240918"}, {"sample": false, "description": "2 TABLET in 1 BOTTLE (71335-2488-8)", "package_ndc": "71335-2488-8", "marketing_start_date": "20240918"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE (71335-2488-9)", "package_ndc": "71335-2488-9", "marketing_start_date": "20240918"}], "brand_name": "Phentermine Hydrochloride", "product_id": "71335-2488_302f8c11-5717-4e3d-a5b2-41794d50c9d1", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "71335-2488", "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": "20240215", "listing_expiration_date": "20261231"}