NDC 71335-1583

ACARBOSE

Acarbose

ACARBOSE is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Acarbose.

Product ID71335-1583_6abd4ad4-4989-4403-a971-35dac770b2f4
NDC71335-1583
Product TypeHuman Prescription Drug
Proprietary NameACARBOSE
Generic NameAcarbose
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-02-01
Marketing CategoryANDA / ANDA
Application NumberANDA091343
Labeler NameBryant Ranch Prepack
Substance NameACARBOSE
Active Ingredient Strength50 mg/1
Pharm Classesalpha Glucosidase Inhibitors [MoA],alpha-Glucosidase Inhibitor [EPC]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 71335-1583-1

30 TABLET in 1 BOTTLE (71335-1583-1)
Marketing Start Date2020-04-27
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "ACARBOSE" or generic name "Acarbose"

NDCBrand NameGeneric Name
0054-0140AcarboseAcarbose
0054-0141AcarboseAcarbose
0054-0142AcarboseAcarbose
11788-039ACARBOSEACARBOSE
11788-040ACARBOSEACARBOSE
11788-041ACARBOSEACARBOSE
23155-147AcarboseAcarbose
23155-148AcarboseAcarbose
23155-149AcarboseAcarbose
42291-130acarboseacarbose
42291-131acarboseacarbose
42291-132acarboseacarbose
43353-951Acarboseacarbose
47781-340Acarboseacarbose
47781-341Acarboseacarbose
47781-342Acarboseacarbose
50090-4115Acarboseacarbose
50090-4116Acarboseacarbose
50090-4952Acarboseacarbose
50090-5088ACARBOSEACARBOSE
50090-5829Acarboseacarbose
68151-0537AcarboseAcarbose
69543-121ACARBOSEACARBOSE
69543-120ACARBOSEACARBOSE
69543-122ACARBOSEACARBOSE
55289-171AcarboseAcarbose
63629-5698AcarboseAcarbose
63629-5697AcarboseAcarbose
64380-759AcarboseAcarbose
64380-760AcarboseAcarbose
64380-758AcarboseAcarbose
72789-131AcarboseAcarbose
72789-132AcarboseAcarbose
72789-133AcarboseAcarbose
71335-1583ACARBOSEACARBOSE
43353-908PrecoseAcarbose
50419-861PrecoseAcarbose
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