Nadolol

Product NDC
31722-349
11-digit product format
317220349
Labeler code
31722
Product ID
31722-349_32deca47-c3a3-4b1e-80ad-22e4b1500282
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Nadolol
Dosage form
TABLET
Route
ORAL
Labeler
Camber, Pharmaceuticals Inc
Application
ANDA203455
Marketing category
ANDA
Marketing start
2016-01-27
Marketing end
0000-00-00
Substance
NADOLOL
Active strength
80 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
31722-349-01EA - Each31722-3492fb2da34-1c21-4824-9b6e-2f4ff7b934f412016-02-04

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
31722-349NADOLOL TABLET [CAMBER, PHARMACEUTICALS INC]1Legacy NDC20160128_54b165a5-23ef-4c44-8971-02b757bba687.zip