01 1Boehringer Ingelheim GmbH
02 1Catalent Pharma Solutions
03 1RP SCHERER GMBH & CO. KG
01 2Germany
02 1U.S.A
01 2Inactive
02 1Blank
01 3Blank
01 3Blank
01 3Blank
01 3Blank
01 112714-901
02 2Blank
01 3Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20707
Submission : 2007-07-10
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17783
Submission : 2004-10-26
Status : Inactive
Type : II
NDC Package Code : 12714-901
Start Marketing Date : 2005-07-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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A Aptivus (Boehringer Ingelheim) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aptivus (Boehringer Ingelheim), including repackagers and relabelers. The FDA regulates Aptivus (Boehringer Ingelheim) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aptivus (Boehringer Ingelheim) API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Aptivus (Boehringer Ingelheim) supplier is an individual or a company that provides Aptivus (Boehringer Ingelheim) active pharmaceutical ingredient (API) or Aptivus (Boehringer Ingelheim) finished formulations upon request. The Aptivus (Boehringer Ingelheim) suppliers may include Aptivus (Boehringer Ingelheim) API manufacturers, exporters, distributors and traders.
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