NDC 71205-855

ACARBOSE

Acarbose

ACARBOSE is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Proficient Rx Lp. The primary component is Acarbose.

Product ID71205-855_203cd13e-8c8d-4782-9e5a-2f9d1b20dd42
NDC71205-855
Product TypeHuman Prescription Drug
Proprietary NameACARBOSE
Generic NameAcarbose
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-02-01
Marketing CategoryANDA /
Application NumberANDA091343
Labeler NameProficient Rx LP
Substance NameACARBOSE
Active Ingredient Strength50 mg/1
Pharm Classesalpha Glucosidase Inhibitors [MoA], alpha-Glucosidase Inhibitor [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 71205-855-00

100 TABLET in 1 BOTTLE (71205-855-00)
Marketing Start Date2022-05-25
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
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.