phentermine hydrochloride
Generic: phentermine hydrochloride
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
phentermine hydrochloride
Generic Name
phentermine hydrochloride
Labeler
proficient rx lp
Dosage Form
CAPSULE
Routes
Active Ingredients
phentermine hydrochloride 30 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
63187-987
Product ID
63187-987_f8e58aea-898e-441f-a256-2bfb18e7fc4d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040875
DEA Schedule
civ
Listing Expiration
2026-12-31
Marketing Start
2012-08-07
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63187987
Hyphenated Format
63187-987
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
ANDA040875 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 mg/1
Packaging
- 7 CAPSULE in 1 BOTTLE (63187-987-07)
- 30 CAPSULE in 1 BOTTLE (63187-987-30)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f8e58aea-898e-441f-a256-2bfb18e7fc4d", "openfda": {"unii": ["0K2I505OTV"], "rxcui": ["900038"], "spl_set_id": ["f2da0b5a-c7d6-48c3-98e9-7c611eb6ff7e"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "7 CAPSULE in 1 BOTTLE (63187-987-07)", "package_ndc": "63187-987-07", "marketing_start_date": "20180301"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (63187-987-30)", "package_ndc": "63187-987-30", "marketing_start_date": "20180301"}], "brand_name": "Phentermine Hydrochloride", "product_id": "63187-987_f8e58aea-898e-441f-a256-2bfb18e7fc4d", "dosage_form": "CAPSULE", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "63187-987", "dea_schedule": "CIV", "generic_name": "Phentermine Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phentermine Hydrochloride", "active_ingredients": [{"name": "PHENTERMINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA040875", "marketing_category": "ANDA", "marketing_start_date": "20120807", "listing_expiration_date": "20261231"}