AMINOPHYLLINE

Orange BookUNIISPLATC R03DA55

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

Identification

ManufacturerHF Acquisition Co LLC, DBA HealthFirst

CountryUS (United States)

ATC codeR03DA55

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 2

ndc11
5166213411
20 mL in 1 VIAL, SINGLE-DOSE (51662-1341-1)
ndc11
5166213413
25 POUCH in 1 CASE (51662-1341-3) / 1 mL in 1 POUCH (51662-1341-2)

Annotations

UNII (FDA Substance ID)

C229N9DX94

AMINOPHYLLINE DIHYDRATE

RxCUI 1298965

Orange Book

A087242

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "C229N9DX94",
    "rxcui": "1298965",
    "inchikey": "FXNJPZOEDHBGEY-UHFFFAOYSA-N",
    "display_name": "AMINOPHYLLINE DIHYDRATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRAVENOUS",
  "spl_meta": {
    "52bbc6cd-4baf-7859-e063-6394a90ac87d": {
      "match": "brand_token",
      "title": "AMINOPHYLLINE INJECTION, SOLUTION [MEDICAL PURCHASING SOLUTIONS, LLC]",
      "spl_version": "1",
      "published_date": "2026-05-28"
    }
  },
  "productid": "51662-1341_1057db94-30a8-224a-e063-6394a90a020d",
  "productndc": "51662-1341",
  "dosage_form": "INJECTION, SOLUTION",
  "orange_book": {
    "appl_no": "087242",
    "products": [
      {
        "rs": true,
        "rld": true,
        "te_code": null,
        "strength": "25MG/ML",
        "product_no": "001",
        "approval_date": "Oct 26, 1983"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "AMINOPHYLLINE DIHYDRATE",
  "proprietary_name": "AMINOPHYLLINE",
  "active_ingred_unit": "mg/mL",
  "application_number": "ANDA087242",
  "marketing_category": "ANDA",
  "nonproprietary_name": "AMINOPHYLLINE",
  "start_marketing_date": "20190210",
  "active_numerator_strength": "25"
}

Related drugs

Other records sharing ATC code R03DA55.

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