Chlorpromazine hydrochloride

Product NDC
64725-1397
11-digit product format
647251397
Labeler code
64725
Product ID
64725-1397_e4d5f9da-e10d-40ca-8abd-66d2de237db1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Chlorpromazine hydrochloride
Dosage form
INJECTION
Route
INTRAMUSCULAR
Labeler
TYA Pharmaceuticals
Application
ANDA083329
Marketing category
ANDA
Marketing start
1974-07-25
Marketing end
0000-00-00
Substance
CHLORPROMAZINE HYDROCHLORIDE
Active strength
25 mg/mL
Pharmacologic classes
Phenothiazines [CS],Phenothiazine [EPC]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
4907e598-fa92-6444-8b2a-22992506f30aProduct name720260202
78470689-2901-bec5-3fa3-182378bb1540Product name320250124
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
a347b2b0-0f41-4d16-ac0d-358db7d523f1Product name120220110
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64725-1397-12020-01-31C16284748780-19d75b9d0-bd16-f424-e053-dadaa90a57ceChlorpromazine Hydrochloride Injection, USP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64725-1397-1Chlorpromazine hydrochloride25 mL in 1 CARTONINJECTION252

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64725-1397CHLORPROMAZINE HYDROCHLORIDE INJECTION [TYA PHARMACEUTICALS]2Legacy NDC, 1 package rows20141028_0e97db69-e09b-407d-8a81-a36cc80fff13.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1730076chlorproMAZINE HCl 25 MG in 1 ML InjectionPSN0e97db69-e09b-407d-8a81-a36cc80fff132
17300761 ML chlorpromazine hydrochloride 25 MG/ML InjectionSCD0e97db69-e09b-407d-8a81-a36cc80fff132
1730076chlorpromazine HCl 25 MG per 1 ML InjectionSY0e97db69-e09b-407d-8a81-a36cc80fff132

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
64725-1397-16472513970125 mL in 1 CARTON25 mlHistorical