methylphenidate hydrochloride (la) (75907-052)

Drug Facts

Product Profile

Brand Name methylphenidate hydrochloride (la)

Generic Name methylphenidate hydrochloride

Labeler dr. reddy's laboratories inc

Dosage Form CAPSULE, EXTENDED RELEASE

Routes

ORAL

Active Ingredients

methylphenidate hydrochloride 40 mg/1

Manufacturer

Dr. Reddy's Laboratories Inc

Identifiers & Regulatory

Product NDC 75907-052

Product ID 75907-052_256aeb9c-b91a-46b9-35fc-94648f5f585c

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA078458

DEA Schedule cii

Listing Expiration 2026-12-31

Marketing Start 2024-12-20

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 75907052

Hyphenated Format 75907-052

Supplemental Identifiers

RxCUI

1806177 1806179 1806183 1806185 1806195

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 (la) (source: ndc)

Generic Name methylphenidate hydrochloride (source: ndc)

Application Number ANDA078458 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

40 mg/1

source: ndc

Packaging

100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (75907-052-01)

source: ndc

Packages (1)

75907-052-01 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (75907-052-01)

Ingredients (1)

methylphenidate hydrochloride (40 mg/1)

Linked Drug Pages (1)

Methylphenidate Hydrochloride (LA) ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "256aeb9c-b91a-46b9-35fc-94648f5f585c", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1806177", "1806179", "1806183", "1806185", "1806195"], "spl_set_id": ["d8c14df4-ac05-d69d-9308-58a51d568329"], "manufacturer_name": ["Dr. Reddy's Laboratories Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (75907-052-01)", "package_ndc": "75907-052-01", "marketing_start_date": "20241220"}], "brand_name": "Methylphenidate Hydrochloride (LA)", "product_id": "75907-052_256aeb9c-b91a-46b9-35fc-94648f5f585c", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "75907-052", "dea_schedule": "CII", "generic_name": "Methylphenidate Hydrochloride", "labeler_name": "Dr. Reddy's Laboratories Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate Hydrochloride (LA)", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA078458", "marketing_category": "ANDA", "marketing_start_date": "20241220", "listing_expiration_date": "20261231"}