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NDC 00409-5555-02 Sodium Bicarbonate 42 mg/mL Details
Sodium Bicarbonate 42 mg/mL
Sodium Bicarbonate is a INTRAVENOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Hospira, Inc.. The primary component is SODIUM BICARBONATE.
Product Information
NDC | 00409-5555 |
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Product ID | 0409-5555_b81f60cb-9cb1-45d5-b27c-424ac1c846b6 |
Associated GPIs | 79050020002010 |
GCN Sequence Number | 001182 |
GCN Sequence Number Description | sodium bicarbonate VIAL 0.5MEQ/ML INTRAVEN |
HIC3 | C0K |
HIC3 Description | BICARBONATE PRODUCING/CONTAINING AGENTS |
GCN | 02790 |
HICL Sequence Number | 000523 |
HICL Sequence Number Description | SODIUM BICARBONATE |
Brand/Generic | Generic |
Proprietary Name | Sodium Bicarbonate |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | SODIUM BICARBONATE |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | INJECTION, SOLUTION |
Route | INTRAVENOUS |
Active Ingredient Strength | 42 |
Active Ingredient Units | mg/mL |
Substance Name | SODIUM BICARBONATE |
Labeler Name | Hospira, Inc. |
Pharmaceutical Class | Alkalinizing Activity [MoA] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA202981 |
Listing Certified Through | 2025-12-31 |
Package
NDC 00409-5555-02 (00409555502)
NDC Package Code | 0409-5555-02 |
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Billing NDC | 00409555502 |
Package | 25 VIAL, SINGLE-USE in 1 TRAY (0409-5555-02) / 5 mL in 1 VIAL, SINGLE-USE (0409-5555-12) |
Marketing Start Date | 2019-10-21 |
NDC Exclude Flag | N |
Pricing Information | N/A |