Hebei started the small package of traditional Chinese medicine decoction pieces to promote the development of Chinese medicine industry

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Hebei started the small package of traditional Chinese medicine decoction pieces to promote the development of Chinese medicine industry

In view of the simple and random packaging of traditional Chinese medicine decoction pieces, which leads to the phenomenon of shoddy filling and doping and falsehood, the Hebei Food and Drug Administration issued a notice requesting the production and operation of Chinese Herbal Pieces from November 1, 2009. Enterprises must use standard material packaging, and the packaging quantity should not exceed 1kg. This indicates that the bulk pieces will be withdrawn from the historical stage in Hebei Province. This will not only help the quality tracking and traceability of Chinese herbal medicines, but also promote the quality of Chinese medicines, promote the development of Chinese medicine industry, and promote Chinese traditional medicine.

Notification requirements:

1. Medical institutions and pharmaceutical retail enterprises must purchase decoction pieces with legal packaging and labeling from legal Chinese medicine decoction pieces production and management enterprises, and check the qualifications of salesmen online, and obtain corresponding certificates and bills.

2. The packaging and labeling of traditional Chinese medicine decoction pieces should meet the four requirements.

1. The packaging materials for traditional Chinese medicine decoction pieces must be packaged in plastic materials that are non-toxic, harmless, transparent and meet the edible standards.

2, the amount of Chinese medicine decoction pieces, according to different types of pieces and customer needs, but more than 1Kg.

3. The Chinese medicine decoction pieces purchased from the decoction piece production enterprises shall be marked with the product name, place of origin, specifications, manufacturer's name, drug production license number, product batch number, production date, and the quality qualified mark; implementation approval number management The Chinese medicine decoction must indicate the approval number.

4. The traditional Chinese medicine decoction pieces purchased from the wholesale foods of the pieces should be marked with the name, specification, place of origin, name of the business enterprise, date of manufacture, date of packaging, and the mark of qualified quality. The Chinese medicine decoction pieces purchased from the decoction piece production enterprises and then sub-packaged and wholesaled must also indicate the name of the manufacturer and the batch number of the production.

This regulation will be implemented from November 1, 2009. Chinese medicine decoction pieces purchased by pharmaceutical companies and medical institutions may continue to be sold until they are used up, but the time shall not exceed December 1, 2010.

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MAIN API  PRODUCTS   USP/BP

PRODUCT  NAME  

CAS NUMBER

SPEVIFICATION

Azithromycin

117772-70-0  

BEP

Cefpirome Sulphate sterile

84957-29-9     

USP JP16

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104376-79-6   

USP31

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64485-93-4  

USP30

Ciprofloxacin  HCL  

85721-33-1

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1405-41-0  

BP

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100986-85-4  

USP27

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859-18-7  

EP6.0

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USP31

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220620-09-7

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EP

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156604-79-4

BP2008

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15687-27-1

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68-89-3

DAB

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38194-50-2   

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163133-43-5

USP28

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154-69-8   

USP28

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84625-61-6   

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147-94-4     

USP31

Leucovorin Calcium

1492-18-8

USP32

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137862-53-4  

USP30

Telmisartan

144701-48-4  

USP31

Rosuvastatin Calcium   

147098-20-2

USP/BP

Pitavastatin Calcium

147526-32-7

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Fluvastatin  

93957-54-1

USP31

Vinpocetine

42971-09-5  

EP6.0

Atazanavir  

198904-31-3

BP

Rosiglitazone

122320-73-4     

USP30

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161973-10-0

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Topiramate   

 97240-79-4      

USP31

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153439-40-8    

Inhouse

Bosentan    

147536-97-8    

Inhouse

D-Cysteine     

921-01-7      

Inhouse

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673-06-3  

Inhouse

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668270-12-0  

Inhouse

Rivaroxaban

366789-02-8

USP

Saxagliptin   

361442-04-8      

USP

Vildagliptin      

274901-16-5       

USP

 

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APIs & Intermediates

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