Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.

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01 1217MF10601
02 1219MF10235
03 1220MF10125
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01 120210722-210-J-1076
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01 122552-0040
02 124002-0024
03 138779-0195
04 149452-1077
05 150909-5102
06 151927-1951
07 152128-161
08 165089-0004
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GDUFA
DMF Review : Reviewed
Rev. Date : 2023-10-25
Pay. Date : 2023-10-03
DMF Number : 37466
Submission : 2022-09-09
Status : Active
Type : II
Date of Issue : 2025-09-03
Valid Till : 2028-09-02
Written Confirmation Number : WC-0161
Address of the Firm :
NDC Package Code : 22552-0040
Start Marketing Date : 2014-12-10
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Symbiotica delivers high-quality APIs through advanced R&D, GMP-certified manufacturing, & trusted global pharmaceutical partnerships.
Certificate Number : R1-CEP 2013-326 - Rev 00
Issue Date : 2020-10-27
Type : Chemical
Substance Number : 810
Status : Valid
Date of Issue : 2025-05-20
Valid Till : 2028-05-22
Written Confirmation Number : 3923/25
Address of the Firm :
NDC Package Code : 52128-161
Start Marketing Date : 2011-11-23
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Insung Trading Co., Ltd.
Registration Date : 2021-07-22
Registration Number : 20210722-210-J-1076
Manufacturer Name : Symbiotica Specialty Ingredients Sdn. Bhd.
Manufacturer Address : No. 518, Jalan Waja 4, Taman Industri Waja, 09000 Kulim, Kedah, Malaysia
Gonane has API manufacturing expertise in new-age Corticosteroids, Hormones and other pharma raw materials.
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
Cerata Pharmaceuticals LLP: WHO-GMP Certified Leading Manufacturer & Exporter of Steroid-Hormone & Peptide APIs From India.
Curia - Accelerating therapies from discovery to commercialization with flexible, scalable CDMO solutions.
GDUFA
DMF Review : Reviewed
Rev. Date : 2023-12-07
Pay. Date : 2023-09-27
DMF Number : 38831
Submission : 2023-09-20
Status : Active
Type : II
Certificate Number : R1-CEP 2002-032 - Rev 01
Issue Date : 2021-08-24
Type : Chemical
Substance Number : 810
Status : Valid
Registration Number : 219MF10235
Registrant's Address : Parque Tecnologico-Parcela 105 Boecillo (Valladolid) Spain
Initial Date of Registration : 2007-07-06
Latest Date of Registration :
NDC Package Code : 65089-0004
Start Marketing Date : 1965-03-03
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
| Available Reg Filing : CN, RU |
Date of Issue : 2022-06-30
Valid Till : 2025-07-02
Written Confirmation Number : WC-0161A2
Address of the Firm :
Date of Issue : 2022-06-30
Valid Till : 2025-07-02
Written Confirmation Number : WC-0161n
Address of the Firm :
Date of Issue : 2022-08-31
Valid Till : 2025-07-02
Written Confirmation Number : WC-0162Amended
Address of the Firm :
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A CELESTONE SOLUSPAN-1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CELESTONE SOLUSPAN-1, including repackagers and relabelers. The FDA regulates CELESTONE SOLUSPAN-1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CELESTONE SOLUSPAN-1 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A CELESTONE SOLUSPAN-1 supplier is an individual or a company that provides CELESTONE SOLUSPAN-1 active pharmaceutical ingredient (API) or CELESTONE SOLUSPAN-1 finished formulations upon request. The CELESTONE SOLUSPAN-1 suppliers may include CELESTONE SOLUSPAN-1 API manufacturers, exporters, distributors and traders.
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We have 38 companies offering CELESTONE SOLUSPAN-1
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