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United States · US · US:0078-0439_00db4d6e-410b-43a1-ab5e-7047f525e68d

Ritalin

In shortageOrange BookUNIISPLATC N06BA04

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerNovartis Pharmaceuticals Corporation
CountryUS (United States)
ATC codeN06BA04
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    0078043905
    100 TABLET in 1 BOTTLE (0078-0439-05)

Annotations

UNII (FDA Substance ID)
4B3SC438HI
METHYLPHENIDATE HYDROCHLORIDE
RxCUI 203188
Orange Book
N010187
ABABAB
DailyMed SPL labels
1 version tracked
FDA shortage
Currently in shortage
Methylphenidate Hydrochloride Tablet, Extended Release
Raw payload (JSON)
{
  "unii": {
    "unii": "4B3SC438HI",
    "rxcui": "203188",
    "inchikey": "JUMYIBMBTDDLNG-OJERSXHUSA-N;JUMYIBMBTDDLNG-QNTKWALQSA-N",
    "display_name": "METHYLPHENIDATE HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "effd952d-ac94-47bb-b107-589a4934dcca": {
      "match": "brand_token",
      "title": "RITALIN LA (METHYLPHENIDATE HYDROCHLORIDE) CAPSULE, EXTENDED RELEASE [NOVARTIS PHARMACEUTICALS CORPORATION]",
      "spl_version": "36",
      "published_date": "2025-10-01"
    }
  },
  "productid": "0078-0439_00db4d6e-410b-43a1-ab5e-7047f525e68d",
  "productndc": "0078-0439",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "010187",
    "products": [
      {
        "rs": false,
        "rld": true,
        "te_code": "AB",
        "strength": "5MG",
        "product_no": "003",
        "approval_date": "Approved Prior to Jan 1, 1982"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": "AB",
        "strength": "10MG",
        "product_no": "006",
        "approval_date": "Approved Prior to Jan 1, 1982"
      },
      {
        "rs": true,
        "rld": true,
        "te_code": "AB",
        "strength": "20MG",
        "product_no": "010",
        "approval_date": "Approved Prior to Jan 1, 1982"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": "CII",
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "METHYLPHENIDATE HYDROCHLORIDE",
  "shortage_reason": "Methylphenidate Hydrochloride Tablet, Extended Release",
  "shortage_status": "current",
  "proprietary_name": "Ritalin",
  "active_ingred_unit": "mg/1",
  "application_number": "NDA010187",
  "marketing_category": "NDA",
  "nonproprietary_name": "methylphenidate hydrochloride",
  "start_marketing_date": "19551231",
  "active_numerator_strength": "5"
}

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