CYPROHEPTADINE HYDROCHLORIDE

Product NDC
50742-190
11-digit product format
507420190
Labeler code
50742
Product ID
50742-190_4357bb59-3551-49fd-8fcf-2d90c801776a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
CYPROHEPTADINE HYDROCHLORIDE
Dosage form
TABLET
Route
ORAL
Labeler
Ingenus Pharmaceuticals LLC
Application
ANDA205087
Marketing category
ANDA
Marketing start
2015-09-23
Substance
CYPROHEPTADINE HYDROCHLORIDE
Active strength
4 mg/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
CYPROHEPTADINE HYDROCHLORIDE
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CYPROHEPTADINE HYDROCHLORIDE4 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiNJ82J0F8QC
Rxcui866144

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9917ef47-291c-0597-9549-0221b002efcdProduct name720210804
67b21aa0-8a78-94d2-63ec-d7e6aa48ff6bProduct name520190821

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50742-190-01CYPROHEPTADINE HYDROCHLORIDE100 in 1 BOTTLE, PLASTICTABLET1006
50742-190-10CYPROHEPTADINE HYDROCHLORIDE1000 in 1 BOTTLE, PLASTICTABLET10006

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50742-190-01EA - Each50742-190c79c471c-97cd-4a64-a427-ca57143f18fe12015-11-12
50742-190-10EA - Each50742-1908ea8b194-8419-4445-b5e6-41d39de04cc612015-11-12

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CYPROHEPTADINE HYDROCHLORIDEACTIVE INGREDIENTNJ82J0F8QCCYPROHEPTADINE HYDROCHLORIDE TABLET [INGENUS PHARMACEUTICALS LLC]1
CYPROHEPTADINEACTIVE MOIETY2YHB6175DOCYPROHEPTADINE HYDROCHLORIDE TABLET [INGENUS PHARMACEUTICALS LLC]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UCYPROHEPTADINE HYDROCHLORIDE TABLET [INGENUS PHARMACEUTICALS LLC]1
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XCYPROHEPTADINE HYDROCHLORIDE TABLET [INGENUS PHARMACEUTICALS LLC]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30CYPROHEPTADINE HYDROCHLORIDE TABLET [INGENUS PHARMACEUTICALS LLC]1
SODIUM STARCH GLYCOLATE TYPE A CORNINACTIVE INGREDIENTAG9B65PV6BCYPROHEPTADINE HYDROCHLORIDE TABLET [INGENUS PHARMACEUTICALS LLC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50742-190CYPROHEPTADINE HYDROCHLORIDE TABLET [INGENUS PHARMACEUTICALS LLC]5Current NDC, Legacy NDC, 2 package rows20200808_56f428c9-8d33-4c91-91d8-1fe194335066.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
866144cyproheptadine HCl 4 MG Oral TabletPSN56f428c9-8d33-4c91-91d8-1fe1943350666
866144cyproheptadine hydrochloride 4 MG Oral TabletSCD56f428c9-8d33-4c91-91d8-1fe1943350666
866144cyproheptadine HCl 4 MG Oral TabletPSN95c03949-0e9a-e3b5-e053-2995a90a56b64
866144cyproheptadine hydrochloride 4 MG Oral TabletSCD95c03949-0e9a-e3b5-e053-2995a90a56b64

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50742-190-0150742019001100 TABLET in 1 BOTTLE, PLASTIC (50742-190-01) 100 tablet2015-09-230000-00-00NoNoCurrent
50742-190-10507420190101000 TABLET in 1 BOTTLE, PLASTIC (50742-190-10) 1000 tablet2015-09-230000-00-00NoNoCurrent