phentermine hydrochloride
Generic: phentermine hydrochloride
Labeler: nucare pharmaceuticals,inc.Drug Facts
Product Profile
Brand Name
phentermine hydrochloride
Generic Name
phentermine hydrochloride
Labeler
nucare pharmaceuticals,inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
phentermine hydrochloride 30 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68071-3535
Product ID
68071-3535_2d3fa192-bcd3-7d2f-e063-6394a90aa73f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040886
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
680713535
Hyphenated Format
68071-3535
Supplemental Identifiers
RxCUI
UPC
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
ANDA040886 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 mg/1
Packaging
- 30 CAPSULE in 1 BOTTLE (68071-3535-3)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2d3fa192-bcd3-7d2f-e063-6394a90aa73f", "openfda": {"upc": ["0368071353532"], "unii": ["0K2I505OTV"], "rxcui": ["900038"], "spl_set_id": ["0b4d847a-fcda-df31-e063-6294a90a0c5e"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (68071-3535-3)", "package_ndc": "68071-3535-3", "marketing_start_date": "20231129"}], "brand_name": "Phentermine Hydrochloride", "product_id": "68071-3535_2d3fa192-bcd3-7d2f-e063-6394a90aa73f", "dosage_form": "CAPSULE", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "68071-3535", "dea_schedule": "CIV", "generic_name": "Phentermine Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phentermine Hydrochloride", "active_ingredients": [{"name": "PHENTERMINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA040886", "marketing_category": "ANDA", "marketing_start_date": "20120807", "listing_expiration_date": "20261231"}