NDC 31722-008

Zafirlukast

Zafirlukast

Zafirlukast is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Camber Pharmaceuticals, Inc.. The primary component is Zafirlukast.

Product ID31722-008_5d30ffab-38a1-411d-94ad-0a15c227d882
NDC31722-008
Product TypeHuman Prescription Drug
Proprietary NameZafirlukast
Generic NameZafirlukast
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2020-09-10
Marketing CategoryANDA / ANDA
Application NumberANDA212475
Labeler NameCamber Pharmaceuticals, Inc.
Substance NameZAFIRLUKAST
Active Ingredient Strength20 mg/1
Pharm ClassesLeukotriene Receptor Antagonists [MoA],Cytochrome P450 2C9 Inhibitors [MoA],Leukotriene Receptor Antagonist [EPC]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 31722-008-01

10 BLISTER PACK in 1 CARTON (31722-008-01) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Marketing Start Date2020-09-10
NDC Exclude FlagN
Sample Package?N

Drug Details

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

NDCBrand NameGeneric Name
0904-6646Zafirlukastzafirlukast
16571-654ZafirlukastZafirlukast
16571-655ZafirlukastZafirlukast Tablets
31722-007ZafirlukastZafirlukast
31722-008ZafirlukastZafirlukast
49884-549Zafirlukastzafirlukast
49884-554Zafirlukastzafirlukast
50268-805ZafirlukastZafirlukast
55111-625ZafirlukastZafirlukast
55111-626ZafirlukastZafirlukast
63629-2102Zafirlukastzafirlukast
64380-187Zafirlukastzafirlukast
64380-188Zafirlukastzafirlukast
68084-059ZafirlukastZafirlukast
68151-1977ZafirlukastZafirlukast
49884-010ACCOLATEzafirlukast
49884-011ACCOLATEzafirlukast
49884-589Accolatezafirlukast
49884-590Accolatezafirlukast
53808-0203ACCOLATEZafirlukast
64380-177ACCOLATEZafirlukast
64380-178ACCOLATEZafirlukast

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