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NDC 55150-0234-10 Polymyxin B 500000 [USP'U]/1 Details
Polymyxin B 500000 [USP'U]/1
Polymyxin B is a INTRAMUSCULAR; INTRATHECAL; INTRAVENOUS; OPHTHALMIC INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Eugia US LLC. The primary component is POLYMYXIN B SULFATE.
Product Information
NDC | 55150-0234 |
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Product ID | 55150-234_ba953500-6973-4b5c-a055-d5ef9d78ca28 |
Associated GPIs | 16100010102105 |
GCN Sequence Number | 009354 |
GCN Sequence Number Description | polymyxin B sulfate VIAL 500K UNIT INJECTION |
HIC3 | W1N |
HIC3 Description | POLYMYXIN ANTIBIOTICS AND DERIVATIVES |
GCN | 41320 |
HICL Sequence Number | 004049 |
HICL Sequence Number Description | POLYMYXIN B SULFATE |
Brand/Generic | Generic |
Proprietary Name | Polymyxin B |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Polymyxin B |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Route | INTRAMUSCULAR; INTRATHECAL; INTRAVENOUS; OPHTHALMIC |
Active Ingredient Strength | 500000 |
Active Ingredient Units | [USP'U]/1 |
Substance Name | POLYMYXIN B SULFATE |
Labeler Name | Eugia US LLC |
Pharmaceutical Class | Polymyxin-class Antibacterial [EPC], Polymyxins [CS] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA206589 |
Listing Certified Through | 2024-12-31 |
Package
NDC 55150-0234-10 (55150023410)
NDC Package Code | 55150-234-10 |
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Billing NDC | 55150023410 |
Package | 10 VIAL in 1 CARTON (55150-234-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL |
Marketing Start Date | 2016-04-04 |
NDC Exclude Flag | N |
Pricing Information | N/A |