Home NDC 61919-732 Losartan Potassium HCTZ
Product NDC 61919-732
11-digit product format 619190732
Labeler code 61919
Product ID 61919-732_94e411c3-44ae-14f5-e053-2995a90ab25f
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Losartan Potassium HCTZ
Dosage form TABLET, FILM COATED
Route ORAL
Labeler DIRECT RX
Application ANDA091629
Marketing category ANDA
Marketing start 2019-04-18
Marketing end 0000-00-00
Substance HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
Active strength 13 mg/1; mg/1
Pharmacologic classes Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
NDC exclude flag No
Listing certified through 2020-12-31
Current FDA listing Historical FDA.report record DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 61919-732-90 Losartan Potassium HCTZ 90 in 1 BOTTLE TABLET, FILM COATED 90 6
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 61919-732 LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED LOSARTAN POTASSIUM HCTZ TABLET, FILM COATED [DIRECT RX] 6 Legacy NDC, 1 package rows 20191015_982c6ccb-f0b2-4e77-8e05-d9f821300740.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 61919-732-90 61919073290 90 TABLET, FILM COATED in 1 BOTTLE (61919-732-90) 2019-04-18 0000-00-00 No No Current