NDC 65862-617

Quinapril

Quinapril Hydrochloride

Quinapril is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Aurobindo Pharma Limited. The primary component is Quinapril Hydrochloride.

Product ID65862-617_0b3b1837-3de4-4c11-a561-ec7d0f10105c
NDC65862-617
Product TypeHuman Prescription Drug
Proprietary NameQuinapril
Generic NameQuinapril Hydrochloride
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2013-04-29
Marketing CategoryANDA / DRUG FOR FURTHER PROCESSING
Application NumberANDA202725
Labeler NameAurobindo Pharma Limited
Substance NameQUINAPRIL HYDROCHLORIDE
Active Ingredient Strength5 mg/1
Pharm ClassesAngiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 65862-617-30

30 TABLET, FILM COATED in 1 BOTTLE (65862-617-30)
Marketing Start Date2013-04-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 65862-617-10 [65862061710]

Quinapril TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA202725
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-04-29

NDC 65862-617-78 [65862061778]

Quinapril TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA202725
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-04-29

NDC 65862-617-90 [65862061790]

Quinapril TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA202725
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2013-04-29

NDC 65862-617-55 [65862061755]

Quinapril TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA202725
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-04-29

NDC 65862-617-30 [65862061730]

Quinapril TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA202725
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-04-29

NDC 65862-617-99 [65862061799]

Quinapril TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA202725
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-04-29

Drug Details

Active Ingredients

IngredientStrength
QUINAPRIL HYDROCHLORIDE5 mg/1

Medicade Reported Pricing

65862061790 QUINAPRIL 5 MG TABLET

Pricing Unit: EA | Drug Type:

NDC Crossover Matching brand name "Quinapril" or generic name "Quinapril Hydrochloride"

NDCBrand NameGeneric Name
21695-393QuinaprilQuinapril
21695-394QuinaprilQuinapril
31722-267QuinaprilQuinapril
31722-268QuinaprilQuinapril
31722-269QuinaprilQuinapril
31722-270QuinaprilQuinapril
43547-410QUINAPRILquinapril
43547-411QUINAPRILquinapril
43547-412QUINAPRILquinapril
43547-413QUINAPRILquinapril
50090-0937QuinaprilQuinapril
50090-2116QuinaprilQuinapril Hydrochloride
68001-187QuinaprilQuinapril
68001-188QuinaprilQuinapril
68001-189QuinaprilQuinapril
68001-260QuinaprilQuinapril
68071-3258QuinaprilQuinapril
68084-899QuinaprilQuinapril
68180-557QuinaprilQuinapril
68180-554QuinaprilQuinapril
68180-558QuinaprilQuinapril
68180-556QuinaprilQuinapril
68788-6894QuinaprilQuinapril
69097-843QuinaprilQuinapril
69097-839QuinaprilQuinapril
69097-841QuinaprilQuinapril
69097-842QuinaprilQuinapril
50090-2117QuinaprilQuinapril
50090-2643QuinaprilQuinapril
55111-624QuinaprilQuinapril
55154-1032QuinaprilQuinapril
55111-621QuinaprilQuinapril
55111-622QuinaprilQuinapril
55111-623QuinaprilQuinapril
62756-313QuinaprilQuinapril
62756-311QuinaprilQuinapril
62756-310QuinaprilQuinapril
62756-312QuinaprilQuinapril
63187-425QuinaprilQuinapril
63629-1241QuinaprilQuinapril
63187-874QuinaprilQuinapril
63304-549QuinaprilQuinapril
63304-548QuinaprilQuinapril
63304-550QuinaprilQuinapril
63304-551QuinaprilQuinapril
65862-619QuinaprilQuinapril
65862-620QuinaprilQuinapril
65862-617QuinaprilQuinapril
65862-618QuinaprilQuinapril
0071-0527Accuprilquinapril hydrochloride
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