Prochlorperazine

Product NDC
66267-176
11-digit product format
662670176
Labeler code
66267
Product ID
66267-176_63264765-9ae5-286c-e053-2a91aa0ad0a9
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Prochlorperazine
Dosage form
SUPPOSITORY
Route
RECTAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA040058
Marketing category
ANDA
Marketing start
1993-11-30
Marketing end
0000-00-00
Substance
PROCHLORPERAZINE
Active strength
25 mg/1
Pharmacologic classes
Phenothiazine [EPC],Phenothiazines [CS]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
66267-176-02EA - Each66267-1768388d3b2-935d-4e12-b3cd-67624d75964e12018-02-20