Labetalol hydrochloride

Product NDC
60429-277
11-digit product format
604290277
Labeler code
60429
Product ID
60429-277_7a07f7b3-78aa-0d61-e053-2a91aa0aa0e3
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Labetalol hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Golden State Medical Supply, Inc.
Application
ANDA075133
Marketing category
ANDA
Marketing start
2013-04-16
Marketing end
0000-00-00
Substance
LABETALOL HYDROCHLORIDE
Active strength
100 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
60429-277-01EA - Each60429-277506d0b15-222a-4623-9bb1-09614bd14ed312013-07-02
60429-277-05EA - Each60429-2770bb2686a-d453-4326-88bf-b18560ddd2c812013-07-02