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NDC 51662-1204-01 AMINOPHYLLINE 25 mg/mL Details
AMINOPHYLLINE 25 mg/mL
AMINOPHYLLINE is a INTRAVENOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by HF Acquisition Co LLC, DBA HealthFirst. The primary component is AMINOPHYLLINE DIHYDRATE.
Product Information
| NDC | 51662-1204 |
|---|---|
| Product ID | 51662-1204_0e739cf0-6ac6-03b2-e063-6294a90a6548 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | AMINOPHYLLINE |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | AMINOPHYLLINE |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | INJECTION, SOLUTION |
| Route | INTRAVENOUS |
| Active Ingredient Strength | 25 |
| Active Ingredient Units | mg/mL |
| Substance Name | AMINOPHYLLINE DIHYDRATE |
| Labeler Name | HF Acquisition Co LLC, DBA HealthFirst |
| Pharmaceutical Class | Methylxanthine [EPC], Xanthines [CS] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA087242 |
| Listing Certified Through | 2025-12-31 |
Package
NDC 51662-1204-01 (51662120401)
| NDC Package Code | 51662-1204-1 |
|---|---|
| Billing NDC | 51662120401 |
| Package | 10 mL in 1 VIAL, SINGLE-DOSE (51662-1204-1) |
| Marketing Start Date | 2018-09-13 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |