Haloperidol Decanoate

Product NDC
70518-1809
11-digit product format
705181809
Labeler code
70518
Product ID
70518-1809_c4bfd77e-dd05-4210-e053-2a95a90a3f4b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Haloperidol Decanoate
Dosage form
INJECTION
Route
INTRAMUSCULAR
Labeler
REMEDYREPACK INC.
Application
ANDA075440
Marketing category
ANDA
Marketing start
2019-01-21
Marketing end
0000-00-00
Substance
HALOPERIDOL DECANOATE
Active strength
100 mg/mL
Pharmacologic classes
Typical Antipsychotic [EPC]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70518-1809-0705181809005 VIAL in 1 CARTON (70518-1809-0) > 1 mL in 1 VIAL (70518-1809-1) 5 vial2019-01-210000-00-00NoNoCurrent