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来自 1 家已认证供应商的 1 条产品

US FDA GMP EU GMP Has US DMF Has CEP No regulatory action Sample available APIs only Excipients only

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Segment determines which GMP annexe and filings apply.

Active Pharmaceutical IngredientsThe substance responsible for the therapeutic effect, as defined by ICH Q7.0Key Starting MaterialsA raw material or intermediate incorporated as a significant structural fragment of the API.0IntermediatesA material produced during API synthesis that undergoes further molecular change before becoming the API.0Pharma Raw MaterialsSolvents, reagents and process chemicals consumed in manufacture but not present in the final product.0ExcipientsInactive substances formulated alongside the API — binders, fillers, coatings and the rest.1Finished Dose FormsProduct ready for patient administration — the packaged, dosed form.0Specialty & Niche ChemicalsHigh-potency, controlled or otherwise specialised materials needing dedicated handling.0

AntidiabeticCardiovascularCNS / NeurologyOncologyAnti-infectivesRespiratoryGastrointestinalAnti-inflammatoryOphthalmologyHormones / SteroidsAntiviralsDermatologyVitamins & Nutraceuticals

A supplier must hold EVERY certificate you select. Each is checked against the issuing authority.

US FDA GMP21 CFR 210/211 — US market1EU GMPEudraGMDP — EU/EEA market0WHO PrequalificationUN, Global Fund, emerging markets0ICH Q7API GMP guide for regulated markets0PMDA (Japan)Japanese market0Health CanadaCanadian market0TGA (Australia)Australian market0ANVISA (Brazil)Brazilian market0SFDA (Saudi Arabia)GCC markets0SAHPRA (South Africa)Sub-Saharan Africa0CDSCO Schedule MIndia domestic0

A filed DMF or CEP is what lets your regulatory team reference this supplier in a submission.

Active US DMF (Type II)Drug Master File filed with the FDAEuropean ASMF filedActive Substance Master FileCEP / COS (EDQM)Ph.Eur. compliance certified by EDQMCoPP availableCertificate of Pharmaceutical Product

Excludes suppliers with a current FDA import alert, an open warning letter, or an EU GMP non-compliance.

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USPBPPh.EurIPJP

%

India1

–USD/kg

kg

days

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Computed from your own requirement — see the score breakdown for the components.

Microcrystalline Cellulose
Aurobindo Pharma · India
CAS
9004-34-6
起订量
500 kg
标准
NF / EP
价格
$2.1–2.8
交货周期
2 weeks
ExcipientsFiller / diluentUS FDA GMPCDSCO

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交易市场

来自 1 家已认证供应商的 1 条产品

新建需求

US FDA GMP EU GMP Has US DMF Has CEP No regulatory action Sample available APIs only Excipients only

Filters

Clear all (1)

Segment determines which GMP annexe and filings apply.

Active Pharmaceutical IngredientsThe substance responsible for the therapeutic effect, as defined by ICH Q7.0Key Starting MaterialsA raw material or intermediate incorporated as a significant structural fragment of the API.0IntermediatesA material produced during API synthesis that undergoes further molecular change before becoming the API.0Pharma Raw MaterialsSolvents, reagents and process chemicals consumed in manufacture but not present in the final product.0ExcipientsInactive substances formulated alongside the API — binders, fillers, coatings and the rest.1Finished Dose FormsProduct ready for patient administration — the packaged, dosed form.0Specialty & Niche ChemicalsHigh-potency, controlled or otherwise specialised materials needing dedicated handling.0

AntidiabeticCardiovascularCNS / NeurologyOncologyAnti-infectivesRespiratoryGastrointestinalAnti-inflammatoryOphthalmologyHormones / SteroidsAntiviralsDermatologyVitamins & Nutraceuticals

A supplier must hold EVERY certificate you select. Each is checked against the issuing authority.

US FDA GMP21 CFR 210/211 — US market1EU GMPEudraGMDP — EU/EEA market0WHO PrequalificationUN, Global Fund, emerging markets0ICH Q7API GMP guide for regulated markets0PMDA (Japan)Japanese market0Health CanadaCanadian market0TGA (Australia)Australian market0ANVISA (Brazil)Brazilian market0SFDA (Saudi Arabia)GCC markets0SAHPRA (South Africa)Sub-Saharan Africa0CDSCO Schedule MIndia domestic0

A filed DMF or CEP is what lets your regulatory team reference this supplier in a submission.

Active US DMF (Type II)Drug Master File filed with the FDAEuropean ASMF filedActive Substance Master FileCEP / COS (EDQM)Ph.Eur. compliance certified by EDQMCoPP availableCertificate of Pharmaceutical Product

Excludes suppliers with a current FDA import alert, an open warning letter, or an EU GMP non-compliance.

Only show these

USPBPPh.EurIPJP

%

India1

–USD/kg

kg

days

Only show these

Computed from your own requirement — see the score breakdown for the components.

Microcrystalline Cellulose
Aurobindo Pharma · India
CAS
9004-34-6
起订量
500 kg
标准
NF / EP
价格
$2.1–2.8
交货周期
2 weeks
ExcipientsFiller / diluentUS FDA GMPCDSCO

交易市场

Microcrystalline Cellulose

交易市场

Microcrystalline Cellulose