NDC 60687-560

Repaglinide

Repaglinide

Repaglinide is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by American Health Packaging. The primary component is Repaglinide.

Product ID60687-560_ac1315f0-ca96-13ec-e053-2a95a90ad2a3
NDC60687-560
Product TypeHuman Prescription Drug
Proprietary NameRepaglinide
Generic NameRepaglinide
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2020-08-01
Marketing CategoryANDA / ANDA
Application NumberANDA203820
Labeler NameAmerican Health Packaging
Substance NameREPAGLINIDE
Active Ingredient Strength1 mg/1
Pharm ClassesGlinide [EPC],Potassium Channel Antagonists [MoA]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 60687-560-21

30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-560-21) > 1 TABLET in 1 BLISTER PACK (60687-560-11)
Marketing Start Date2020-08-01
NDC Exclude FlagN
Sample Package?N

Drug Details

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

NDCBrand NameGeneric Name
0378-3122Repagliniderepaglinide
0378-3123Repagliniderepaglinide
0574-0240RepaglinideREPAGLINIDE
0574-0241RepaglinideREPAGLINIDE
0574-0242RepaglinideREPAGLINIDE
51079-539Repagliniderepaglinide
51991-853REPAGLINIDEREPAGLINIDE
51991-854REPAGLINIDEREPAGLINIDE
51991-855REPAGLINIDEREPAGLINIDE
57237-157RepaglinideRepaglinide
57237-158RepaglinideRepaglinide
57237-159RepaglinideRepaglinide
57664-745RepaglinideRepaglinide
57664-747RepaglinideRepaglinide
60429-484REPAGLINIDEREPAGLINIDE
60429-485REPAGLINIDEREPAGLINIDE
60429-486REPAGLINIDEREPAGLINIDE
68084-967RepaglinideRepaglinide
68084-954RepaglinideRepaglinide
65862-670RepaglinideRepaglinide
65862-671RepaglinideRepaglinide
65862-672RepaglinideRepaglinide
0169-0081Prandinrepaglinide
0169-0082Prandinrepaglinide
0169-0084Prandinrepaglinide

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