methylphenidate hydrochloride

Generic: methylphenidate hydrochloride

Labeler: camber pharmaceutical inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methylphenidate hydrochloride
Generic Name methylphenidate hydrochloride
Labeler camber pharmaceutical inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methylphenidate hydrochloride 10 mg/1

Manufacturer
Camber Pharmaceutical Inc

Identifiers & Regulatory

Product NDC 31722-174
Product ID 31722-174_85610552-360d-4ae3-b160-0819534f8220
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207416
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2015-10-01

Pharmacologic Class

Classes
central nervous system stimulant [epc] central nervous system stimulation [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 31722174
Hyphenated Format 31722-174

Supplemental Identifiers

RxCUI
1091150 1091392 1091497
UNII
4B3SC438HI

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name methylphenidate hydrochloride (source: ndc)
Generic Name methylphenidate hydrochloride (source: ndc)
Application Number ANDA207416 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (31722-174-01)
  • 500 TABLET in 1 BOTTLE (31722-174-05)
source: ndc

Packages (2)

31722-174-01 100 TABLET in 1 BOTTLE (31722-174-01) 31722-174-05 500 TABLET in 1 BOTTLE (31722-174-05)

Ingredients (1)

methylphenidate hydrochloride (10 mg/1)

Linked Drug Pages (1)

METHYLPHENIDATE HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "85610552-360d-4ae3-b160-0819534f8220", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1091150", "1091392", "1091497"], "spl_set_id": ["778190da-1528-4def-94bf-ee23ee5268a5"], "manufacturer_name": ["Camber Pharmaceutical Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (31722-174-01)", "package_ndc": "31722-174-01", "marketing_start_date": "20151001"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (31722-174-05)", "package_ndc": "31722-174-05", "marketing_start_date": "20151001"}], "brand_name": "METHYLPHENIDATE HYDROCHLORIDE", "product_id": "31722-174_85610552-360d-4ae3-b160-0819534f8220", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "31722-174", "dea_schedule": "CII", "generic_name": "METHYLPHENIDATE HYDROCHLORIDE", "labeler_name": "Camber Pharmaceutical Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METHYLPHENIDATE HYDROCHLORIDE", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA207416", "marketing_category": "ANDA", "marketing_start_date": "20151001", "listing_expiration_date": "20261231"}