MILNACIPRAN HYDROCHLORIDE

Orange BookUNIISPLATC N06AX17

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

Identification

ManufacturerCamber Pharmaceuticals, Inc.

CountryUS (United States)

ATC codeN06AX17

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 2

ndc11
3172284932
10 BLISTER PACK in 1 CARTON (31722-849-32) / 10 TABLET, FILM COATED in 1 BLISTER PACK
ndc11
3172284960
60 TABLET, FILM COATED in 1 BOTTLE (31722-849-60)

Annotations

UNII (FDA Substance ID)

RNZ43O5WW5

MILNACIPRAN HYDROCHLORIDE

RxCUI 30003

Orange Book

A205147

ABABABAB

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "RNZ43O5WW5",
    "rxcui": "30003",
    "inchikey": "XNCDYJFPRPDERF-PBCQUBLHSA-N;XNCDYJFPRPDERF-NQQJLSKUSA-N",
    "display_name": "MILNACIPRAN HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "b66b1850-0d2a-41d6-b0ad-c676166394c7": {
      "match": "brand_token",
      "title": "MILNACIPRAN HYDROCHLORIDE TABLET, FILM COATED [GLENMARK PHARMACEUTICALS INC., USA]",
      "spl_version": "4",
      "published_date": "2026-03-26"
    }
  },
  "productid": "31722-849_4cbf720f-9cdf-7cfe-e063-6394a90a6d84",
  "productndc": "31722-849",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "205147",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "12.5MG",
        "product_no": "001",
        "approval_date": "Oct 3, 2024"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "25MG",
        "product_no": "002",
        "approval_date": "Oct 3, 2024"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "50MG",
        "product_no": "003",
        "approval_date": "Oct 3, 2024"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "100MG",
        "product_no": "004",
        "approval_date": "Oct 3, 2024"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "MILNACIPRAN HYDROCHLORIDE",
  "proprietary_name": "MILNACIPRAN HYDROCHLORIDE",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA205147",
  "marketing_category": "ANDA",
  "nonproprietary_name": "MILNACIPRAN HYDROCHLORIDE",
  "start_marketing_date": "20260319",
  "active_numerator_strength": "100"
}

Related drugs

Other records sharing ATC code N06AX17.

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