PROCHLORPERAZINE MALEATE

Product NDC: 50090-2242
11-digit product format: 500902242
Labeler code: 50090
Product ID: 50090-2242_9fa30784-054e-4d2c-bdbb-39c6e3f65ede
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Prochlorperazine Maleate
Dosage form: TABLET
Route: ORAL
Labeler: A-S Medication Solutions
Application: ANDA040268
Marketing category: ANDA
Marketing start: 1998-03-01
Marketing end: 0000-00-00
Substance: PROCHLORPERAZINE MALEATE
Active strength: 5 mg/1
Pharmacologic classes: Phenothiazine [EPC],Phenothiazines [CS]
NDC exclude flag: No
Listing certified through: 2022-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
50090-2242-0	2023-02-07	C162847	48780-1	f386c649-f3ff-0266-e053-dadaa90a7c1a	92bfff06-f2d3-495a-9c5e-6e292fe45853
50090-2242-0	2023-01-30	C162847	48780-1	f386c649-f3ff-0266-e053-dadaa90a7c1a	92bfff06-f2d3-495a-9c5e-6e292fe45853

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
50090-2242-0	EA - Each	50090-2242	16e0b5da-15ef-4a2b-96db-7e24b29d75e0	1	2019-02-13

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
50090-2242-0	50090224200	10 TABLET in 1 BOTTLE (50090-2242-0)	10 tablet	2015-11-24	0000-00-00	No	No	Current