Nadolol

Product NDC: 63629-6942
11-digit product format: 636296942
Labeler code: 63629
Product ID: 63629-6942_61bfac78-7e45-4cc4-8d69-57fbb971c72f
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: nadolol
Dosage form: TABLET
Route: ORAL
Labeler: Bryant Ranch Prepack
Application: ANDA074172
Marketing category: ANDA
Marketing start: 1993-10-31
Marketing end: 0000-00-00
Substance: NADOLOL
Active strength: 20 mg/1
Pharmacologic classes: Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
NDC exclude flag: No
Listing certified through: 2021-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
63629-6942-1	2020-10-16	C162847	48780-1	9d75b9d0-5638-f424-e053-dadaa90a57ce	1cc1b542-9015-4bd2-8d31-54aa2292050e
63629-6942-1	2020-01-31	C162847	48780-1	9d75b9d0-5638-f424-e053-dadaa90a57ce	1cc1b542-9015-4bd2-8d31-54aa2292050e

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
FEN504330V	NADOLOL	42200-33-9	NADOLOL

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63629-6942-1	63629694201	30 TABLET in 1 BOTTLE (63629-6942-1)	30 tablet	2016-03-08	0000-00-00	No	No	Current