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NDC 23155-0313-31 Acetazolamide 500 mg/5mL Details
Acetazolamide 500 mg/5mL
Acetazolamide is a INTRAVENOUS INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Heritage Pharmaceuticals Labs Inc. d/b/a Avet Pharmaceuticals Labs Inc.. The primary component is ACETAZOLAMIDE SODIUM.
Product Information
NDC | 23155-0313 |
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Product ID | 23155-313_997907e5-6f68-4cf2-beee-c0e84213d55d |
Associated GPIs | 37100010102105 |
GCN Sequence Number | 008163 |
GCN Sequence Number Description | acetazolamide sodium VIAL 500 MG INJECTION |
HIC3 | R1E |
HIC3 Description | CARBONIC ANHYDRASE INHIBITORS |
GCN | 34680 |
HICL Sequence Number | 003640 |
HICL Sequence Number Description | ACETAZOLAMIDE SODIUM |
Brand/Generic | Generic |
Proprietary Name | Acetazolamide |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Acetazolamide |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Route | INTRAVENOUS |
Active Ingredient Strength | 500 |
Active Ingredient Units | mg/5mL |
Substance Name | ACETAZOLAMIDE SODIUM |
Labeler Name | Heritage Pharmaceuticals Labs Inc. d/b/a Avet Pharmaceuticals Labs Inc. |
Pharmaceutical Class | Carbonic Anhydrase Inhibitor [EPC], Carbonic Anhydrase Inhibitors [MoA], Sulfonamides [CS] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA202693 |
Listing Certified Through | 2024-12-31 |
Package
NDC 23155-0313-31 (23155031331)
NDC Package Code | 23155-313-31 |
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Billing NDC | 23155031331 |
Package | 5 mL in 1 VIAL, GLASS (23155-313-31) |
Marketing Start Date | 2021-10-06 |
NDC Exclude Flag | N |
Pricing Information | N/A |