Urabe Daikanbo Pharmaceutical Co., Ltd. | Tablet Supplements / Capsule SupplementsOEM/ODM Manufacturing (Fukuoka)
Food OEMOfficial Site Verified1761-74 Oaza ChikoVerified Jun 2026
EstablishedODM SupportHACCPGMPOrganic JAS
Service
OEM/ODM
Min lot
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Lead time
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Founded
1790
Certifications:3
Features of Urabe Daikanbo Pharmaceutical Co., Ltd.
Urabe Daikanbo Pharmaceutical Co., Ltd. is a 1790-established food OEM/ODM manufacturer based in Fukuoka.They handle manufacturing of Tablet Supplements, Capsule Supplements, Powder & Granule Supplements, Drink Supplements, Jelly & Gummy Supplements and more.They hold certifications including Health-Food GMP, HACCP, Organic JAS, demonstrating a well-established quality management system.
Recommended For
- Those wanting to outsource product planning and development
- Those who prioritize quality management and safety
- Those looking to develop organic products
- Those seeking experienced, well-established manufacturers
About Urabe Daikanbo Pharmaceutical Co., Ltd. OEM Manufacturing
Long-established kampo (traditional Chinese medicine) pharmaceutical company founded in 1790 (Kansei 2) with over 230 years of history. Develops OEM contract manufacturing of health food and supplements at its GMP-compliant directly operated factory, leveraging pharmaceutical manufacturing know-how. Supports diverse dosage forms including tablets, capsules, granules, drinks and jellies. Organic JAS and HACCP certified.
Business Activities of Urabe Daikanbo Pharmaceutical Co., Ltd.
- Planning
- manufacturing
- wholesale
- and retail of health food supplements
- Planning
- manufacturing
- wholesale
- and retail of quasi-drugs
- Planning
- manufacturing
- wholesale
- and retail of cosmetics
- Planning
- manufacturing
- wholesale
- and retail of general food products
Urabe Daikanbo Pharmaceutical Co., Ltd. Features & Strengths
- 1790年創業・230年以上の歴史
- 漢方の老舗
- GMP適合直営工場
- 有機JAS認証取得
Urabe Daikanbo Pharmaceutical Co., Ltd. Certifications & Equipment
Health-Food GMPHACCPOrganic JAS
Equipment details could not be confirmed from publicly available information. Please refer to the manufacturer's official website for details.
Locations of Urabe Daikanbo Pharmaceutical Co., Ltd.
Factory Locations
本社工場
福岡県直方市大字知古1761-74
· 造粒・顆粒加工、打錠、ハードカプセル充填、分包加工、包装・梱包
· 健康食品GMP適合工場、有機JAS認証、菓子製造業営業許可
Offices
通販事業部
〒813-0062 福岡県福岡市東区松島3-27-15
Company History of Urabe Daikanbo Pharmaceutical Co., Ltd.
- 1790
(Kansei 2): Yamana family, the predecessor entity, established a pharmaceutical business; October 1957: Uribe Taikanado Pharmaceutical Co., Ltd. was incorporated
Awards & Recognition of Urabe Daikanbo Pharmaceutical Co., Ltd.
Excellent Centennial Company Award
Group Companies of Urabe Daikanbo Pharmaceutical Co., Ltd.
大連永佐貿易有限公司(中国・大連市)
Urabe Daikanbo Pharmaceutical Co., Ltd. Supported Categories
Learn about this category
FAQ about Urabe Daikanbo Pharmaceutical Co., Ltd.
Where is Urabe Daikanbo Pharmaceutical Co., Ltd. located?
Urabe Daikanbo Pharmaceutical Co., Ltd. is located in Fukuoka, 直方市, 福岡県直方市大字知古1761-74.
What types of products can Urabe Daikanbo Pharmaceutical Co., Ltd. manufacture?
They handle manufacturing of Tablet Supplements, Capsule Supplements, Powder & Granule Supplements, Drink Supplements, Jelly & Gummy Supplements, Functional Foods (FFC / Tokuho) and more.
Does Urabe Daikanbo Pharmaceutical Co., Ltd. support ODM?
Urabe Daikanbo Pharmaceutical Co., Ltd. supports OEM/ODM.
What certifications and quality standards does Urabe Daikanbo Pharmaceutical Co., Ltd. have?
They are certified for Health-Food GMP, HACCP, Organic JAS.
Common Pre-Order Questions
Frequently asked questions from buyers before placing an OEM order. Manufacturer-specific details can be confirmed via a quote request.
What are typical minimum order quantities (MOQ)?
MOQs vary by manufacturer, but listed partners handle anything from small lots (100–1,000 units) up to large-scale production (100,000+). The lower bound depends on raw material sourcing and packaging specs, so confirm exact MOQs in your quote request.
How long does it take from quote to delivery?
Quote replies typically take 3–7 business days. From there, mass-production delivery (including prototyping) generally takes 2–4 months. New formulation development or certification work can extend this past six months. Final schedule is set during the quote phase.
Are prototype or sample fees charged?
Most manufacturers charge for prototypes (typically a few hundred USD up), but the cost is often credited back once mass production is confirmed. Existing-formula samples are sometimes free. Policies vary, so confirm in advance.
Can we sign an NDA?
Yes, generally. Quote requests routed through OEM JAPAN can be covered by an NDA before formulation or recipe details are shared. Either the manufacturer's or the buyer's NDA template can be used.
What shelf-life can be set for food products?
Depends on format and sterilization. Typical targets: retort foods 1–2 years, frozen 1 year, refrigerated 30–90 days, ambient baked goods 90–180 days. Shelf-life is fixed after stability testing (microbial and sensory).
Can allergen labeling and ingredient specs be accommodated?
Yes. Most manufacturers manage the 8 mandatory + 20 recommended allergen items, and some operate gluten-free, dairy-free, or vegan dedicated lines. Share any required ingredient specs in the quote request.
Are HACCP or food-safety certifications in place?
HACCP is mandatory for Japanese food manufacturers, so nearly all listed partners operate HACCP or equivalent systems. You can also filter for upper-tier certifications such as FSSC 22000, ISO 22000, JAS, or Organic JAS.
Contents
Basic Information
Location
1761-74 Oaza Chiko
Founded
1790
Official Website
https://corporate.urabe-taikando.co.jp/Show all company info
Representative
代表取締役 永岡 訓二
Incorporated
10/1957
Capital
2,900万円
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