METHYLPHENIDATE HYDROCHLORIDE

In shortageOrange BookUNIISPLATC N06BA04

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerBryant Ranch Prepack

CountryUS (United States)

ATC codeN06BA04

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 5

ndc11
7133512191
30 TABLET in 1 BOTTLE (71335-1219-1)
ndc11
7133512192
100 TABLET in 1 BOTTLE (71335-1219-2)
ndc11
7133512193
90 TABLET in 1 BOTTLE (71335-1219-3)
ndc11
7133512194
60 TABLET in 1 BOTTLE (71335-1219-4)
ndc11
7133512195
120 TABLET in 1 BOTTLE (71335-1219-5)

Annotations

UNII (FDA Substance ID)

4B3SC438HI

METHYLPHENIDATE HYDROCHLORIDE

RxCUI 203188

Orange Book

A207416

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": {
    "f7a7ffd1-bc30-4db8-8391-dddf76acd639": {
      "match": "brand_token",
      "title": "METHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE [RHODES PHARMACEUTICALS LLC]",
      "spl_version": "8",
      "published_date": "2026-06-01"
    }
  },
  "productid": "71335-1219_6183e88c-f148-4ee3-a49c-6e7aee7009bc",
  "productndc": "71335-1219",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "207416",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "5MG",
        "product_no": "001",
        "approval_date": "Sep 22, 2015"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "10MG",
        "product_no": "002",
        "approval_date": "Sep 22, 2015"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "20MG",
        "product_no": "003",
        "approval_date": "Sep 22, 2015"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": "CII",
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "METHYLPHENIDATE HYDROCHLORIDE",
  "shortage_reason": "Methylphenidate Hydrochloride Tablet, Extended Release",
  "shortage_status": "current",
  "proprietary_name": "METHYLPHENIDATE HYDROCHLORIDE",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA207416",
  "marketing_category": "ANDA",
  "nonproprietary_name": "METHYLPHENIDATE HYDROCHLORIDE",
  "start_marketing_date": "20151001",
  "active_numerator_strength": "20"
}

Related drugs

Other records sharing ATC code N06BA04.

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