lomaira

Generic: phentermine hydrochloride

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

Drug Facts

Product Profile

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

phentermine hydrochloride 8 mg/1

Manufacturer
KVK-TECH, INC.

Identifiers & Regulatory

Product NDC 10702-001
Product ID 10702-001_0ce01306-ef7f-563f-e063-6394a90a52b7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203495
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2016-09-12

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 10702001
Hyphenated Format 10702-001

Supplemental Identifiers

RxCUI
826919 1810304
UPC
0310702001091
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 lomaira (source: ndc)
Generic Name phentermine hydrochloride (source: ndc)
Application Number ANDA203495 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 8 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (10702-001-03)
  • 60 TABLET in 1 BOTTLE (10702-001-06)
  • 90 TABLET in 1 BOTTLE (10702-001-09)
  • 1000 TABLET in 1 BOTTLE (10702-001-10)
  • 250 TABLET in 1 BOTTLE (10702-001-25)
  • 500 TABLET in 1 BOTTLE (10702-001-50)
source: ndc

Packages (6)

10702-001-03 30 TABLET in 1 BOTTLE (10702-001-03) 10702-001-06 60 TABLET in 1 BOTTLE (10702-001-06) 10702-001-09 90 TABLET in 1 BOTTLE (10702-001-09) 10702-001-10 1000 TABLET in 1 BOTTLE (10702-001-10) 10702-001-25 250 TABLET in 1 BOTTLE (10702-001-25) 10702-001-50 500 TABLET in 1 BOTTLE (10702-001-50)

Ingredients (1)

phentermine hydrochloride (8 mg/1)

Linked Drug Pages (1)

LOMAIRA ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0ce01306-ef7f-563f-e063-6394a90a52b7", "openfda": {"upc": ["0310702001091"], "unii": ["0K2I505OTV"], "rxcui": ["826919", "1810304"], "spl_set_id": ["cde9fb09-e5af-434d-8874-e4f9f974d893"], "manufacturer_name": ["KVK-TECH, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (10702-001-03)", "package_ndc": "10702-001-03", "marketing_start_date": "20160912"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (10702-001-06)", "package_ndc": "10702-001-06", "marketing_start_date": "20160912"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (10702-001-09)", "package_ndc": "10702-001-09", "marketing_start_date": "20160912"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (10702-001-10)", "package_ndc": "10702-001-10", "marketing_start_date": "20160912"}, {"sample": false, "description": "250 TABLET in 1 BOTTLE (10702-001-25)", "package_ndc": "10702-001-25", "marketing_start_date": "20160912"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (10702-001-50)", "package_ndc": "10702-001-50", "marketing_start_date": "20160912"}], "brand_name": "LOMAIRA", "product_id": "10702-001_0ce01306-ef7f-563f-e063-6394a90a52b7", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "10702-001", "dea_schedule": "CIV", "generic_name": "Phentermine Hydrochloride", "labeler_name": "KVK-TECH, INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LOMAIRA", "active_ingredients": [{"name": "PHENTERMINE HYDROCHLORIDE", "strength": "8 mg/1"}], "application_number": "ANDA203495", "marketing_category": "ANDA", "marketing_start_date": "20160912", "listing_expiration_date": "20261231"}