FDA.reportPublic FDA data

Application 207875

Type
ANDA
Sponsor
SUN PHARM

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001ALBUTEROL SULFATE AND IPRATROPIUM BROMIDEALBUTEROL SULFATE; IPRATROPIUM BROMIDESOLUTION;INHALATIONEQ 0.083% BASE;0.017%NoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
47335-756Ipratropium Bromide and Albuterol SulfateIpratropium Bromide and Albuterol SulfateSun Pharmaceutical Industries, Inc.ANDACurrent
47335-756Ipratropium Bromide and Albuterol SulfateIpratropium Bromide and Albuterol SulfateSun Pharmaceutical Industries, Inc.ANDACurrent
50090-6288Ipratropium Bromide and Albuterol SulfateIpratropium Bromide and Albuterol SulfateA-S Medication SolutionsANDACurrent
71205-726Ipratropium Bromide and Albuterol SulfateIpratropium Bromide and Albuterol SulfateProficient Rx LPANDACurrent