phentermine hydrochloride
Generic: phentermine hydrochloride
Labeler: directrxDrug Facts
Product Profile
Brand Name
phentermine hydrochloride
Generic Name
phentermine hydrochloride
Labeler
directrx
Dosage Form
CAPSULE
Routes
Active Ingredients
phentermine hydrochloride 30 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72189-253
Product ID
72189-253_2c28de82-39db-9df3-e063-6394a90ac7f9
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA205019
DEA Schedule
civ
Listing Expiration
2026-12-31
Marketing Start
2021-08-25
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72189253
Hyphenated Format
72189-253
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
ANDA205019 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 mg/1
Packaging
- 30 CAPSULE in 1 BOTTLE (72189-253-30)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c28de82-39db-9df3-e063-6394a90ac7f9", "openfda": {"unii": ["0K2I505OTV"], "rxcui": ["900038"], "spl_set_id": ["ca683656-16a6-9602-e053-2a95a90aa895"], "manufacturer_name": ["DirectRx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (72189-253-30)", "package_ndc": "72189-253-30", "marketing_start_date": "20210825"}], "brand_name": "PHENTERMINE HYDROCHLORIDE", "product_id": "72189-253_2c28de82-39db-9df3-e063-6394a90ac7f9", "dosage_form": "CAPSULE", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "72189-253", "dea_schedule": "CIV", "generic_name": "PHENTERMINE HYDROCHLORIDE", "labeler_name": "DirectRx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PHENTERMINE HYDROCHLORIDE", "active_ingredients": [{"name": "PHENTERMINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA205019", "marketing_category": "ANDA", "marketing_start_date": "20210825", "listing_expiration_date": "20261231"}