NDC 0591-2406

Ambrisentan

Ambrisentan

Ambrisentan is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Actavis Pharma, Inc.. The primary component is Ambrisentan.

Product ID0591-2406_1f011d26-5710-408d-a0fd-1cf9ee5cbc4c
NDC0591-2406
Product TypeHuman Prescription Drug
Proprietary NameAmbrisentan
Generic NameAmbrisentan
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2019-04-30
Marketing CategoryANDA / DRUG FOR FURTHER PROCESSING
Application NumberANDA208252
Labeler NameActavis Pharma, Inc.
Substance NameAMBRISENTAN
Active Ingredient Strength10 mg/1
Pharm ClassesEndothelin Receptor Antagonist [EPC],Endothelin Receptor Antagonists [MoA]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0591-2406-30

30 TABLET, FILM COATED in 1 BOTTLE (0591-2406-30)
Marketing Start Date2019-04-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0591-2406-30 [00591240630]

Ambrisentan TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA208252
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2019-04-30

Drug Details

Active Ingredients

IngredientStrength
AMBRISENTAN10 mg/1

NDC Crossover Matching brand name "Ambrisentan" or generic name "Ambrisentan"

NDCBrand NameGeneric Name
0378-4270Ambrisentanambrisentan
0378-4271Ambrisentanambrisentan
0591-2405AmbrisentanAmbrisentan
0591-2406AmbrisentanAmbrisentan
42291-018AMBRISENTANAMBRISENTAN
42291-019AMBRISENTANAMBRISENTAN
42794-051AMBRISENTANAMBRISENTAN
42794-052AMBRISENTANAMBRISENTAN
47335-236ambrisentanambrisentan
47335-237ambrisentanambrisentan
49884-353AmbrisentanAmbrisentan
49884-354AmbrisentanAmbrisentan
59651-494ambrisentanambrisentan
59651-495ambrisentanambrisentan
60505-4552AmbrisentanAMBRISENTAN
60505-4553AmbrisentanAMBRISENTAN
69097-386AmbrisentanAmbrisentan
69097-387AmbrisentanAmbrisentan
70710-1179AmbrisentanAmbrisentan
70710-1180AmbrisentanAmbrisentan
70771-1363AmbrisentanAmbrisentan
70771-1364AmbrisentanAmbrisentan
76282-684AmbrisentanAmbrisentan
76282-685AmbrisentanAmbrisentan
61958-0801LetairisAMBRISENTAN
61958-0802LetairisAMBRISENTAN

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.