NDC 68071-1910

Glimepiride

Glimepiride

Glimepiride is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Nucare Pharmaceuticals, I. The primary component is Glimepiride.

Product ID68071-1910_7bd38248-60ea-1f7b-e053-2991aa0a88ec
NDC68071-1910
Product TypeHuman Prescription Drug
Proprietary NameGlimepiride
Generic NameGlimepiride
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2007-08-23
Marketing CategoryANDA / ANDA
Application NumberANDA078181
Labeler NameNuCare Pharmaceuticals, I
Substance NameGLIMEPIRIDE
Active Ingredient Strength2 mg/1
Pharm ClassesSulfonylurea [E
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 68071-1910-3

30 TABLET in 1 BOTTLE (68071-1910-3)
Marketing Start Date2016-12-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68071-1910-9 [68071191009]

Glimepiride TABLET
Marketing CategoryANDA
Application NumberANDA078181
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-12-27

NDC 68071-1910-3 [68071191003]

Glimepiride TABLET
Marketing CategoryANDA
Application NumberANDA078181
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-12-27

NDC 68071-1910-6 [68071191006]

Glimepiride TABLET
Marketing CategoryANDA
Application NumberANDA078181
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-12-27

NDC 68071-1910-8 [68071191008]

Glimepiride TABLET
Marketing CategoryANDA
Application NumberANDA078181
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-12-27

Drug Details

Pharmacological Class

  • Sulfonylurea [EPC]
  • Sulfonylurea Compounds [CS]

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

NDCBrand NameGeneric Name
0093-7254GlimepirideGlimepiride
0093-7255GlimepirideGlimepiride
0093-7256GlimepirideGlimepiride
0378-4011Glimepirideglimepiride
0378-4012Glimepirideglimepiride
0378-4013Glimepirideglimepiride
0440-6564GlimepirideGlimepiride
0440-6565GlimepirideGlimepiride
0440-6566GlimepirideGlimepiride
0615-6575GlimepirideGlimepiride
0615-6576GlimepirideGlimepiride
0615-7523GlimepirideGlimepiride
0615-8332GlimepirideGlimepiride
0615-8333GlimepirideGlimepiride
0615-8334GlimepirideGlimepiride
10544-217GlimepirideGlimepiride
10544-219GlimepirideGlimepiride
16571-773GlimepirideGlimepiride
16571-774GlimepirideGlimepiride
16571-775GlimepirideGlimepiride
16729-001GlimepirideGlimepiride
16729-002GlimepirideGlimepiride
16729-003GlimepirideGlimepiride
21695-746GlimepirideGlimepiride
21695-747GlimepirideGlimepiride
21695-993GlimepirideGlimepiride
33261-831GlimepirideGlimepiride
33261-892GlimepirideGlimepiride
33261-961GlimepirideGlimepiride
35356-896GlimepirideGlimepiride
42571-100GlimepirideGlimepiride
68001-179GlimepirideGlimepiride
68001-177GlimepirideGlimepiride
68001-178GlimepirideGlimepiride
68071-1942GlimepirideGlimepiride
68071-1910GlimepirideGlimepiride
68071-3024GlimepirideGlimepiride
68071-1991GlimepirideGlimepiride
68071-3068GlimepirideGlimepiride
68071-3239GlimepirideGlimepiride
68084-327GlimepirideGlimepiride
68084-326GlimepirideGlimepiride
68084-788GlimepirideGlimepiride
68645-572GlimepirideGlimepiride
68645-573GlimepirideGlimepiride
68788-6801GlimepirideGlimepiride
68788-6818GlimepirideGlimepiride
68788-6436GlimepirideGlimepiride
68788-6411GlimepirideGlimepiride
69452-129GlimepirideGlimepiride

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