phentermine hydrochloride

Generic: phentermine hydrochloride

Labeler: kvk-tech, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name phentermine hydrochloride
Generic Name phentermine hydrochloride
Labeler kvk-tech, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

phentermine hydrochloride 30 mg/1

Manufacturer
KVK-Tech, Inc.

Identifiers & Regulatory

Product NDC 10702-028
Product ID 10702-028_1662a72d-c285-b644-e063-6294a90a7333
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
appetite suppression [pe] increased sympathetic activity [pe] sympathomimetic amine anorectic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 10702028
Hyphenated Format 10702-028

Supplemental Identifiers

RxCUI
900038 968766
UPC
0310702027107 0310702028104 0310702026100
UNII
0K2I505OTV

Packaging Origin

Original Packager
true

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (10702-028-01)
  • 30 CAPSULE in 1 BOTTLE (10702-028-03)
  • 1000 CAPSULE in 1 BOTTLE (10702-028-10)
source: ndc

Packages (3)

10702-028-01 100 CAPSULE in 1 BOTTLE (10702-028-01) 10702-028-03 30 CAPSULE in 1 BOTTLE (10702-028-03) 10702-028-10 1000 CAPSULE in 1 BOTTLE (10702-028-10)

Ingredients (1)

phentermine hydrochloride (30 mg/1)

Linked Drug Pages (1)

Phentermine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1662a72d-c285-b644-e063-6294a90a7333", "openfda": {"upc": ["0310702027107", "0310702028104", "0310702026100"], "unii": ["0K2I505OTV"], "rxcui": ["900038", "968766"], "spl_set_id": ["b963f7bb-fa65-4e28-81c9-282fbe70a6a6"], "manufacturer_name": ["KVK-Tech, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (10702-028-01)", "package_ndc": "10702-028-01", "marketing_start_date": "20120807"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (10702-028-03)", "package_ndc": "10702-028-03", "marketing_start_date": "20120807"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (10702-028-10)", "package_ndc": "10702-028-10", "marketing_start_date": "20120807"}], "brand_name": "Phentermine Hydrochloride", "product_id": "10702-028_1662a72d-c285-b644-e063-6294a90a7333", "dosage_form": "CAPSULE", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "10702-028", "dea_schedule": "CIV", "generic_name": "Phentermine Hydrochloride", "labeler_name": "KVK-Tech, Inc.", "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"}