aminophylline

Generic: aminophylline

Labeler: hf acquisition co llc, dba healthfirst
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name aminophylline
Generic Name aminophylline
Labeler hf acquisition co llc, dba healthfirst
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

aminophylline dihydrate 25 mg/mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1341
Product ID 51662-1341_1057db94-30a8-224a-e063-6394a90a020d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA087242
Listing Expiration 2026-12-31
Marketing Start 2019-02-10

Pharmacologic Class

Classes
methylxanthine [epc] xanthines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621341
Hyphenated Format 51662-1341

Supplemental Identifiers

RxCUI
1724666
UNII
C229N9DX94

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 aminophylline (source: ndc)
Generic Name aminophylline (source: ndc)
Application Number ANDA087242 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 25 mg/mL
source: ndc
Packaging
  • 20 mL in 1 VIAL, SINGLE-DOSE (51662-1341-1)
  • 25 POUCH in 1 CASE (51662-1341-3) / 1 mL in 1 POUCH (51662-1341-2)
source: ndc

Packages (2)

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

Ingredients (1)

aminophylline dihydrate (25 mg/mL)

Linked Drug Pages (1)

AMINOPHYLLINE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "1057db94-30a8-224a-e063-6394a90a020d", "openfda": {"unii": ["C229N9DX94"], "rxcui": ["1724666"], "spl_set_id": ["819207a2-0c37-b275-e053-2a91aa0afb36"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "20 mL in 1 VIAL, SINGLE-DOSE (51662-1341-1)", "package_ndc": "51662-1341-1", "marketing_start_date": "20190210"}, {"sample": false, "description": "25 POUCH in 1 CASE (51662-1341-3)  / 1 mL in 1 POUCH (51662-1341-2)", "package_ndc": "51662-1341-3", "marketing_start_date": "20201027"}], "brand_name": "AMINOPHYLLINE", "product_id": "51662-1341_1057db94-30a8-224a-e063-6394a90a020d", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Methylxanthine [EPC]", "Xanthines [CS]"], "product_ndc": "51662-1341", "generic_name": "AMINOPHYLLINE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMINOPHYLLINE", "active_ingredients": [{"name": "AMINOPHYLLINE DIHYDRATE", "strength": "25 mg/mL"}], "application_number": "ANDA087242", "marketing_category": "ANDA", "marketing_start_date": "20190210", "listing_expiration_date": "20261231"}