FDA.reportPublic FDA data

Amlodipine and Benazepril Hydrochloride

Product NDC
51655-213
11-digit product format
516550213
Labeler code
51655
Product ID
51655-213_48d2a75b-7672-5a6d-e063-6294a90a18b8
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Amlodipine and Benazepril Hydrochloride
Dosage form
CAPSULE
Route
ORAL
Labeler
Northwind Health Company, LLC
Application
ANDA202239
Marketing category
ANDA
Marketing start
2022-10-20
Substance
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Active strength
10; 20 mg/1; mg/1
Pharmacologic classes
Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Decreased Blood Pressure [PE], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Amlodipine and Benazepril Hydrochloride
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AMLODIPINE BESYLATE10 mg/1
BENAZEPRIL HYDROCHLORIDE20 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii864V2Q084H, N1SN99T69T
Rxcui898342

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fa898d56-9495-d6f0-309b-68a5d8e3914aProduct name420260305
c19ec24d-2c40-4b8d-7c20-500ffa3660a1Product name320260303
b15e9aa6-d523-ca97-480e-570e0543a342Product name420251024
265792b3-b999-c010-7364-a7db20b9d4d9Product name520250515
14c2c15b-f823-4ada-a40e-a440544294dcProduct name120221207
a72887ef-d675-499f-af4b-78688f6855cdProduct name120191002
a4484670-2869-6416-f6ff-03b1b3cbd1b0Product name220190415
4a27501f-a987-48a5-99b4-e983d4744d76Product name720181211
18600d07-613d-bf9c-2711-fe40c06f3393Product name520180703
bded1554-44de-900a-5297-403365d6d4b2Product name320170110
55bffd21-17e1-ff02-2e8f-1f9a532b9502Product name220150320
1f1c6e4b-bbad-4649-afd1-7a1d671db4b1Product name120150316
63ab5fbf-2a6b-c41d-051a-39e845d718b1Product name120140508
7613b1a5-acb6-4e5e-6048-c44deeeb1212Product name120140508
b9fbc696-7d55-c52e-4f12-7e3d99cd2db4Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51655-213-26Amlodipine and Benazepril Hydrochloride90 in 1 BOTTLE, PLASTICCAPSULE903
51655-213-52Amlodipine and Benazepril Hydrochloride30 in 1 BOTTLE, PLASTICCAPSULE303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51655-213AMLODIPINE AND BENAZEPRIL HYDROCHLORIDE CAPSULE [NORTHWIND PHARMACEUTICALS, LLC]2Current NDC, 2 package rows20230706_f2b56630-4e3a-6f9c-e053-2a95a90a4650.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
898342amLODIPine besylate 10 MG / benazepril HCl 20 MG Oral CapsulePSNf2b56630-4e3a-6f9c-e053-2a95a90a46503
898342amlodipine 10 MG / benazepril hydrochloride 20 MG Oral CapsuleSCDf2b56630-4e3a-6f9c-e053-2a95a90a46503
898342amlodipine (as amlodipine besylate) 10 MG / benazepril hydrochloride 20 MG Oral CapsuleSYf2b56630-4e3a-6f9c-e053-2a95a90a46503
898342Amlodipine 10 MG / BZP hydrochloride 20 MG Oral CapsuleSYf2b56630-4e3a-6f9c-e053-2a95a90a46503

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
51655-213-265165502132690 CAPSULE in 1 BOTTLE, PLASTIC (51655-213-26) 90 capsule2022-10-20NoNoHistorical
51655-213-525165502135230 CAPSULE in 1 BOTTLE, PLASTIC (51655-213-52) 30 capsule2023-05-02NoNoHistorical