 |
ISBN
| 9781138103771 | |
DDC
| 615.19 | |
Tác giả CN
| Niazi, Sarfaraz K. | |
Nhan đề
| Handbook of pharmaceutical manufacturing formulations. Volume 5, Over-the-counter products / Sarfaraz K. Niazi | |
Lần xuất bản
| 3rd ed. | |
Thông tin xuất bản
| Boca Raton, FL : CRC Press, 2020 | |
Mô tả vật lý
| 444 pages. : illustrations ; cm. | |
Phụ chú
| Includes index. | |
Tóm tắt
| The Handbook of Pharmaceutical Manufacturing Formulations, Third Edition is an authoritative and practical guide to the art and science of formulating drugs for commercial manufacturing. With thoroughly revised and expanded content, this six-volume set compiles data from FDA new drug applications, patent applications, and other sources of generic and proprietary formulations to cover the broad spectrum of GMP formulations and issues in using these formulations in a commercial setting. A must-have collection for pharmaceutical manufacturers, educational institutions, and regulatory authorities, this is an excellent platform for drug companies to benchmark their products and for generic companies to formulate drugs coming off patent | |
Từ khóa tự do
| Drug formulations | |
Từ khóa tự do
| Drug production processes | |
Từ khóa tự do
| Pharmaceutical manufacturing | |
Từ khóa tự do
| Dosage forms | |
Từ khóa tự do
| Pharmaceutical technology | |
Từ khóa tự do
| Quality control in pharmaceuticals | |
Từ khóa tự do
| Industrial pharmacy | |
Khoa
| Khoa Khoa học Ứng dụng và Công nghệ | |
Địa chỉ
| Thư Viện Đại học Nguyễn Tất Thành |
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| 100 | |aNiazi, Sarfaraz K. |
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| 245 | |aHandbook of pharmaceutical manufacturing formulations. |nVolume 5, |pOver-the-counter products / |cSarfaraz K. Niazi |
|---|
| 250 | |a3rd ed. |
|---|
| 260 | |aBoca Raton, FL : |bCRC Press, |c2020 |
|---|
| 300 | |a444 pages. : |billustrations ; |ccm. |
|---|
| 500 | |aIncludes index. |
|---|
| 520 | |aThe Handbook of Pharmaceutical Manufacturing Formulations, Third Edition is an authoritative and practical guide to the art and science of formulating drugs for commercial manufacturing. With thoroughly revised and expanded content, this six-volume set compiles data from FDA new drug applications, patent applications, and other sources of generic and proprietary formulations to cover the broad spectrum of GMP formulations and issues in using these formulations in a commercial setting. A must-have collection for pharmaceutical manufacturers, educational institutions, and regulatory authorities, this is an excellent platform for drug companies to benchmark their products and for generic companies to formulate drugs coming off patent |
|---|
| 653 | |aDrug formulations |
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| 653 | |aDrug production processes |
|---|
| 653 | |aPharmaceutical manufacturing |
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| 653 | |aDosage forms |
|---|
| 653 | |aPharmaceutical technology |
|---|
| 653 | |aQuality control in pharmaceuticals |
|---|
| 653 | |aIndustrial pharmacy |
|---|
| 690 | |aKhoa Khoa học Ứng dụng và Công nghệ |
|---|
| 691 | |aHóa dược |
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| 852 | |aThư Viện Đại học Nguyễn Tất Thành |
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