methylphenidate hydrochloride

Generic: methylphenidate hydrochloride

Labeler: kvk-tech, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methylphenidate hydrochloride
Generic Name methylphenidate hydrochloride
Labeler kvk-tech, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methylphenidate hydrochloride 5 mg/1

Manufacturer
KVK-TECH, INC.

Identifiers & Regulatory

Product NDC 10702-100
Product ID 10702-100_476dd35a-34a9-02dd-e063-6394a90a912a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206932
DEA Schedule cii
Listing Expiration 2027-12-31
Marketing Start 2017-05-11

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 10702100
Hyphenated Format 10702-100

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 ANDA206932 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (10702-100-01)
source: ndc

Packages (1)

10702-100-01 100 TABLET in 1 BOTTLE (10702-100-01)

Ingredients (1)

methylphenidate hydrochloride (5 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": "476dd35a-34a9-02dd-e063-6394a90a912a", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1091150", "1091392", "1091497"], "spl_set_id": ["1bf37f9f-29cf-4b09-9c81-eb369e35a042"], "manufacturer_name": ["KVK-TECH, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (10702-100-01)", "package_ndc": "10702-100-01", "marketing_start_date": "20170511"}], "brand_name": "Methylphenidate Hydrochloride", "product_id": "10702-100_476dd35a-34a9-02dd-e063-6394a90a912a", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "10702-100", "dea_schedule": "CII", "generic_name": "Methylphenidate Hydrochloride", "labeler_name": "KVK-TECH, INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate Hydrochloride", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA206932", "marketing_category": "ANDA", "marketing_start_date": "20170511", "listing_expiration_date": "20271231"}