01 1Olon S.p.A
02 1Piramal Pharma Solutions
03 1Sifavitor srl
04 1Sumitomo Chemical
05 2Blank
01 2Italy
02 1Japan
03 1U.S.A
04 2Blank
01 2Active
02 3Inactive
03 1Blank
01 6Blank
01 1218MF10957
02 5Blank
01 1WC-0123
02 5Blank
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GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14195
Submission : 1999-06-07
Status : Active
Type : II
Registration Number : 218MF10957
Registrant's Address : Strada Rivoltana Km 6/7 20090 Rodano Milano Italy
Initial Date of Registration : 2006-12-01
Latest Date of Registration : --
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16904
Submission : 2003-10-16
Status : Active
Type : II
Date of Issue : 2022-06-29
Valid Till : 2025-07-02
Written Confirmation Number : WC-0123
Address of the Firm :
NDC Package Code : 65085-0029
Start Marketing Date : 2004-06-30
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (2kg/2kg)
Marketing Category : BULK INGREDIENT
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5113
Submission : 1983-09-15
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11519
Submission : 1995-05-19
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9652
Submission : 1992-05-11
Status : Inactive
Type : II
NDC Package Code : 17337-0525
Start Marketing Date : 2020-02-27
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Levobunolol Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levobunolol Hydrochloride, including repackagers and relabelers. The FDA regulates Levobunolol Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levobunolol Hydrochloride API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Levobunolol Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Levobunolol Hydrochloride supplier is an individual or a company that provides Levobunolol Hydrochloride active pharmaceutical ingredient (API) or Levobunolol Hydrochloride finished formulations upon request. The Levobunolol Hydrochloride suppliers may include Levobunolol Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Levobunolol Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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