Corgard

Product NDC: 27505-102
11-digit product format: 275050102
Labeler code: 27505
Product ID: 27505-102_edfe5dbf-1a62-4cd6-e053-2995a90a3521
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: nadolol
Dosage form: TABLET
Route: ORAL
Labeler: US WorldMeds, LLC
Application: NDA018063
Marketing category: NDA
Marketing start: 2016-04-01
Marketing end: 2023-01-31
Substance: NADOLOL
Active strength: 80 mg/1
Pharmacologic classes: Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
NDC exclude flag: No
Listing certified through: 0000-00-00
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
27505-102-01	2021-10-12	C162847	48780-1	c7ccaba7-1eff-fd44-e053-dadaa90aa01b	bcae071c-bd67-4fa9-be40-3325ebf04119
27505-102-01	2021-07-23	C162847	48780-1	c7ccaba7-1eff-fd44-e053-dadaa90aa01b	bcae071c-bd67-4fa9-be40-3325ebf04119

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
27505-102-01	EA - Each	27505-102	ac39b390-e33d-4b51-b8cd-61b7fb291a96	1	2016-04-04

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
27505-102-01	27505010201	100 TABLET in 1 BOTTLE (27505-102-01)	100 tablet	2016-04-01	0000-00-00	No	No	Current