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NDC 00338-9558-10 Eptifibatide 75 mg/100mL Details
Eptifibatide 75 mg/100mL
Eptifibatide is a INTRAVENOUS INJECTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Baxter Healthcare Corporation. The primary component is EPTIFIBATIDE.
Product Information
NDC | 00338-9558 |
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Product ID | 0338-9558_adec2ba9-b744-4539-98c8-8c9b0be57abe |
Associated GPIs | 85153030002010 |
GCN Sequence Number | 079535 |
GCN Sequence Number Description | eptifibatide PLAST. BAG 75MG/100ML INTRAVEN |
HIC3 | M9P |
HIC3 Description | PLATELET AGGREGATION INHIBITORS |
GCN | 46043 |
HICL Sequence Number | 018422 |
HICL Sequence Number Description | EPTIFIBATIDE |
Brand/Generic | Generic |
Proprietary Name | Eptifibatide |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Eptifibatide |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | INJECTION |
Route | INTRAVENOUS |
Active Ingredient Strength | 75 |
Active Ingredient Units | mg/100mL |
Substance Name | EPTIFIBATIDE |
Labeler Name | Baxter Healthcare Corporation |
Pharmaceutical Class | Decreased Platelet Aggregation [PE], Platelet Aggregation Inhibitor [EPC] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA208554 |
Listing Certified Through | 2024-12-31 |
Package
NDC 00338-9558-10 (00338955810)
NDC Package Code | 0338-9558-10 |
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Billing NDC | 00338955810 |
Package | 1 VIAL, SINGLE-DOSE in 1 CARTON (0338-9558-10) / 100 mL in 1 VIAL, SINGLE-DOSE |
Marketing Start Date | 2019-02-01 |
NDC Exclude Flag | N |
Pricing Information | N/A |