Chlorpromazine Hydrochloride

Product NDC
0832-6019
11-digit product format
008326019
Labeler code
0832
Product ID
0832-6019_787f32b3-e4f6-424d-a2c0-d249b5bbcd93
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Chlorpromazine Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Upsher-Smith Laboratories, LLC
Application
ANDA084113
Marketing category
ANDA
Marketing start
2011-08-03
Substance
CHLORPROMAZINE HYDROCHLORIDE
Active strength
50 mg/1
Pharmacologic classes
Phenothiazine [EPC], Phenothiazines [CS]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Chlorpromazine Hydrochloride
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CHLORPROMAZINE HYDROCHLORIDE50 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii9WP59609J6
Rxcui991039, 991044, 991188, 991194, 991336

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
4907e598-fa92-6444-8b2a-22992506f30aProduct name720260202
78470689-2901-bec5-3fa3-182378bb1540Product name320250124
a347b2b0-0f41-4d16-ac0d-358db7d523f1Product name120220110

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0832-6019-00Chlorpromazine Hydrochloride100 in 1 BOTTLETABLET, FILM COATED1004
0832-6019-01Chlorpromazine Hydrochloride1 in 1 CARTONTABLET, FILM COATED14
0832-6019-10Chlorpromazine Hydrochloride1000 in 1 BOTTLETABLET, FILM COATED10004
0832-6019-89Chlorpromazine Hydrochloride100 in 1 BLISTER PACKTABLET, FILM COATED1004

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0832-6019-00EA - Each0832-60197f990276-ec81-46e8-bb7f-6a0cc6f1452a12022-06-06
0832-6019-01EA - Each0832-601901aebba5-23eb-497e-864d-a4054ffc5de112022-02-07
0832-6019-10EA - Each0832-6019797b5c48-9162-48e5-a4b4-dafaa3d789bd12022-06-06
0832-6019-89EA - Each0832-60190c40acda-7395-4187-b1c5-9693c3c75b6812022-02-07

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0832-6019CHLORPROMAZINE HYDROCHLORIDE TABLET, FILM COATED [UPSHER-SMITH LABORATORIES, LLC]2Current NDC, Legacy NDC, 4 package rows20230531_5ae79c1e-f523-4358-9f8b-7382a03d59bc.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
991039chlorproMAZINE HCl 10 MG Oral TabletPSN5ae79c1e-f523-4358-9f8b-7382a03d59bc4
991044chlorproMAZINE HCl 100 MG Oral TabletPSN5ae79c1e-f523-4358-9f8b-7382a03d59bc4
991188chlorproMAZINE HCl 200 MG Oral TabletPSN5ae79c1e-f523-4358-9f8b-7382a03d59bc4
991194chlorproMAZINE HCl 25 MG Oral TabletPSN5ae79c1e-f523-4358-9f8b-7382a03d59bc4
991336chlorproMAZINE HCl 50 MG Oral TabletPSN5ae79c1e-f523-4358-9f8b-7382a03d59bc4
991039chlorpromazine hydrochloride 10 MG Oral TabletSCD5ae79c1e-f523-4358-9f8b-7382a03d59bc4
991044chlorpromazine hydrochloride 100 MG Oral TabletSCD5ae79c1e-f523-4358-9f8b-7382a03d59bc4
991188chlorpromazine hydrochloride 200 MG Oral TabletSCD5ae79c1e-f523-4358-9f8b-7382a03d59bc4
991194chlorpromazine hydrochloride 25 MG Oral TabletSCD5ae79c1e-f523-4358-9f8b-7382a03d59bc4
991336chlorpromazine hydrochloride 50 MG Oral TabletSCD5ae79c1e-f523-4358-9f8b-7382a03d59bc4

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0832-6019-0000832601900100 TABLET, FILM COATED in 1 BOTTLE (0832-6019-00) 2021-08-060000-00-00NoNoCurrent
0832-6019-01008326019011 BLISTER PACK in 1 CARTON (0832-6019-01) / 100 TABLET, FILM COATED in 1 BLISTER PACK (0832-6019-89) 1 blister pack2021-08-060000-00-00NoNoCurrent
0832-6019-10008326019101000 TABLET, FILM COATED in 1 BOTTLE (0832-6019-10) 2021-08-060000-00-00NoNoCurrent
0832-6019-8900832601989100 in 1 BLISTER PACKHistorical