terazosin

Product NDC
50090-7851
11-digit product format
500907851
Labeler code
50090
Product ID
50090-7851_bba25161-4506-4e35-a98a-deff97b5d23f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
terazosin
Dosage form
CAPSULE
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA075614
Marketing category
ANDA
Marketing start
2021-04-30
Substance
TERAZOSIN HYDROCHLORIDE
Active strength
1 mg/1
Pharmacologic classes
Adrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
terazosin
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
TERAZOSIN HYDROCHLORIDE1 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiD32S14F082
Rxcui313215

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50090-7851-0terazosin30 in 1 BOTTLECAPSULE301
50090-7851-1terazosin90 in 1 BOTTLECAPSULE901

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-7851-0EA - Each50090-785125b84014-c072-4315-8df2-0e7f995af6e412026-02-05
50090-7851-1EA - Each50090-78510a2d38bf-a3e0-4e78-80d8-212dc53bcf4212026-02-05

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
50090-7851-05009078510030 CAPSULE in 1 BOTTLE (50090-7851-0) 30 capsule2026-01-08NoNoHistorical
50090-7851-15009078510190 CAPSULE in 1 BOTTLE (50090-7851-1) 90 capsule2026-01-08NoNoHistorical