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NDC 70954-0034-20 Acetazolamide 250 mg/1 Details
Acetazolamide 250 mg/1
Acetazolamide is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by ANI Pharmaceuticals, Inc.. The primary component is ACETAZOLAMIDE.
MedlinePlus Drug Summary
Acetazolamide is used to treat glaucoma, a condition in which increased pressure in the eye can lead to gradual loss of vision. Acetazolamide decreases the pressure in the eye. Acetazolamide is also used to reduce the severity and duration of symptoms (upset stomach, headache, shortness of breath, dizziness, drowsiness, and fatigue) of altitude (mountain) sickness. Acetazolamide is used with other medicines to reduce edema (excess fluid retention) and to help control seizures in certain types of epilepsy. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
Related Packages: 70954-0034-20Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Acetazolamide
Product Information
| NDC | 70954-0034 |
|---|---|
| Product ID | 70954-034_a304c648-f1bf-468d-a704-f4d72216f7a0 |
| Associated GPIs | 37100010000310 |
| GCN Sequence Number | 008166 |
| GCN Sequence Number Description | acetazolamide TABLET 250 MG ORAL |
| HIC3 | R1E |
| HIC3 Description | CARBONIC ANHYDRASE INHIBITORS |
| GCN | 34722 |
| HICL Sequence Number | 003641 |
| HICL Sequence Number Description | ACETAZOLAMIDE |
| Brand/Generic | Generic |
| Proprietary Name | Acetazolamide |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Acetazolamide |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 250 |
| Active Ingredient Units | mg/1 |
| Substance Name | ACETAZOLAMIDE |
| Labeler Name | ANI Pharmaceuticals, Inc. |
| Pharmaceutical Class | Carbonic Anhydrase Inhibitor [EPC], Carbonic Anhydrase Inhibitors [MoA], Sulfonamides [CS] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA210588 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 70954-0034-20 (70954003420)
| NDC Package Code | 70954-034-20 |
|---|---|
| Billing NDC | 70954003420 |
| Package | 1000 TABLET in 1 BOTTLE (70954-034-20) |
| Marketing Start Date | 2019-10-17 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |