FDA.reportPublic FDA data

METHYLPHENIDATE HYDROCHLORIDE

Product NDC
31722-174
11-digit product format
317220174
Labeler code
31722
Product ID
31722-174_85610552-360d-4ae3-b160-0819534f8220
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
METHYLPHENIDATE HYDROCHLORIDE
Dosage form
TABLET
Route
ORAL
Labeler
Camber Pharmaceutical Inc
Application
ANDA207416
Marketing category
ANDA
Marketing start
2015-10-01
Substance
METHYLPHENIDATE HYDROCHLORIDE
Active strength
10 mg/1
Pharmacologic classes
Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE]
DEA schedule
CII
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
METHYLPHENIDATE HYDROCHLORIDE10 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii4B3SC438HI
Rxcui1091150, 1091392, 1091497

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
143536be-f21a-464c-bc5a-163f5c171815Product name220250626
fd4d0878-dcea-3832-288e-e3bbbbe580ffProduct name920240516
435f0341-cf24-41d5-8fbf-c909821e5596Product name120230313
c9b6eabb-08d7-bb2d-e81a-06be3590b436Product name220221216
67aa32c6-44f4-50de-64dd-643e8caf420dProduct name620210622
50b24f34-96fa-4f1e-b262-b0baf4a4a440Product name420210513
cf83c421-eebe-4de2-b1a2-fd96e3dbfcf8Product name120200128
166d1d2d-dd55-4fdf-82e2-b83a3c5347c1Product name120190828
343a61d5-785d-cc27-a43a-0779da054d88Product name320190828
7607489b-cd15-3103-f3b1-d4283574d250Product name220190614
407f0cce-da29-4050-a512-2cabe9e5692dProduct name920190611
f7f4bf1e-7c67-46c6-8c42-9beb1a06b38eProduct name220190415
190572d9-6c7b-4b40-8172-c1b5f802c20fProduct name120180724
2948856e-f76e-d380-d9ed-b317efafbc98Product name520180423
c0aa09de-7aa1-4a98-8f70-62ec3c97c695Product name120170803
3317aade-2d6e-f159-9fe6-e8385a825178Product name320160829
0fe52203-83a7-4fed-a91f-8e47a22cf1d3Product name120160111

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
31722-174-01METHYLPHENIDATE HYDROCHLORIDE100 in 1 BOTTLETABLET1009
31722-174-05METHYLPHENIDATE HYDROCHLORIDE500 in 1 BOTTLETABLET5009

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
31722-174-01EA - Each31722-174bb408fea-5c99-4f8a-98a1-bf2cddba7df212016-06-14

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
METHYLPHENIDATE HYDROCHLORIDEACTIVE INGREDIENT4B3SC438HIMETHYLPHENIDATE HYDROCHLORIDE TABLET [CAMBER PHARMACEUTICALS INC.]1
METHYLPHENIDATEACTIVE MOIETY207ZZ9QZ49METHYLPHENIDATE HYDROCHLORIDE TABLET [CAMBER PHARMACEUTICALS INC.]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UMETHYLPHENIDATE HYDROCHLORIDE TABLET [CAMBER PHARMACEUTICALS INC.]1
COLLOIDAL SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4METHYLPHENIDATE HYDROCHLORIDE TABLET [CAMBER PHARMACEUTICALS INC.]1
D&C YELLOW NO. 10INACTIVE INGREDIENT35SW5USQ3GMETHYLPHENIDATE HYDROCHLORIDE TABLET [CAMBER PHARMACEUTICALS INC.]1
FD&C GREEN NO. 3INACTIVE INGREDIENT3P3ONR6O1SMETHYLPHENIDATE HYDROCHLORIDE TABLET [CAMBER PHARMACEUTICALS INC.]1
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XMETHYLPHENIDATE HYDROCHLORIDE TABLET [CAMBER PHARMACEUTICALS INC.]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30METHYLPHENIDATE HYDROCHLORIDE TABLET [CAMBER PHARMACEUTICALS INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554METHYLPHENIDATE HYDROCHLORIDE TABLET [CAMBER PHARMACEUTICALS INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
31722-174METHYLPHENIDATE HYDROCHLORIDE TABLET [CAMBER PHARMACEUTICAL INC]8Current NDC, Legacy NDC, 2 package rows20241012_778190da-1528-4def-94bf-ee23ee5268a5.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1091150methylphenidate HCl 10 MG Oral TabletPSN778190da-1528-4def-94bf-ee23ee5268a59
1091392methylphenidate HCl 20 MG Oral TabletPSN778190da-1528-4def-94bf-ee23ee5268a59
1091497methylphenidate HCl 5 MG Oral TabletPSN778190da-1528-4def-94bf-ee23ee5268a59
1091150methylphenidate hydrochloride 10 MG Oral TabletSCD778190da-1528-4def-94bf-ee23ee5268a59
1091392methylphenidate hydrochloride 20 MG Oral TabletSCD778190da-1528-4def-94bf-ee23ee5268a59
1091497methylphenidate hydrochloride 5 MG Oral TabletSCD778190da-1528-4def-94bf-ee23ee5268a59
1091150methylphenidate HCl 10 MG Oral TabletPSN9e7967c8-d323-160d-e053-2995a90a323e5
1091392methylphenidate HCl 20 MG Oral TabletPSN9e7967c8-d323-160d-e053-2995a90a323e5
1091150methylphenidate hydrochloride 10 MG Oral TabletSCD9e7967c8-d323-160d-e053-2995a90a323e5
1091392methylphenidate hydrochloride 20 MG Oral TabletSCD9e7967c8-d323-160d-e053-2995a90a323e5

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
31722-174-0131722017401100 TABLET in 1 BOTTLE (31722-174-01) 100 tablet2015-10-010000-00-00NoNoCurrent
31722-174-0531722017405500 TABLET in 1 BOTTLE (31722-174-05) 500 tablet2015-10-010000-00-00NoNoCurrent