Clonidine Hydrochloride

Product NDC
55289-074
11-digit product format
552890074
Labeler code
55289
Product ID
55289-074_7b207415-b010-9ab7-e053-2a91aa0a1902
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
clonidine hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
PD-Rx Pharmaceuticals, Inc.
Application
ANDA070317
Marketing category
ANDA
Marketing start
1987-06-09
Marketing end
0000-00-00
Substance
CLONIDINE HYDROCHLORIDE
Active strength
0 mg/1
Pharmacologic classes
Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
55289-074-15EA - Each55289-074ae35bfdc-7fe0-4e03-991b-c07150c5de4512012-07-24
55289-074-30EA - Each55289-074020aa543-09ab-4276-b3b5-f7f49288fa9d12012-07-24
55289-074-60EA - Each55289-0749d7a99fa-09b4-40f5-8d7a-6e25da8b335d12012-07-24
55289-074-90EA - Each55289-074d8744adf-72e7-4333-9dd7-4e3cf9c3a3bb12012-07-24