Haloperidol Decanoate

Product NDC
0703-7023
11-digit product format
007037023
Labeler code
0703
Product ID
0703-7023_0ca22830-67fa-49ec-842b-e1846c0e162c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Haloperidol Decanoate
Dosage form
INJECTION
Route
INTRAMUSCULAR
Labeler
Teva Parenteral Medicines, Inc.
Application
ANDA075393
Marketing category
ANDA
Marketing start
1999-07-01
Marketing end
2020-08-31
Substance
HALOPERIDOL DECANOATE
Active strength
100 mg/mL
Pharmacologic classes
Typical Antipsychotic [EPC]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0703-7023-01ML - Milliliter0703-70231943e3f8-e52d-4e64-ae4f-e23775da3b9c12012-07-24