Haloperidol

Product NDC: 58118-1079
11-digit product format: 581181079
Labeler code: 58118
Product ID: 58118-1079_8d7d12d0-b683-19ba-e053-2995a90a2612
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Haloperidol
Dosage form: TABLET
Route: ORAL
Labeler: Clinical Solutions Wholesale, LLC
Application: ANDA077580
Marketing category: ANDA
Marketing start: 2008-01-03
Marketing end: 0000-00-00
Substance: HALOPERIDOL
Active strength: 5 mg/1
Pharmacologic classes: Typical Antipsychotic [EPC]
NDC exclude flag: No
Listing certified through: 2020-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
58118-1079-8	2021-01-29	C162847	48780-1	ba0f9c33-12db-a910-e053-dadaa90a0b85	c7c15230-dd37-4eb2-8e0b-46a4f5e4b1df

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
58118-1079	HALOPERIDOL TABLET [CLINICAL SOLUTIONS WHOLESALE, LLC]	3	Legacy NDC	20190713_c7c15230-dd37-4eb2-8e0b-46a4f5e4b1df.zip