52125-070 : Diamox 500 mg 12 Hr Extended Release Capsule
NDC: | 52125-070 |
Labeler: | Remedyrepack Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | Diamox Sequels |
Dosage Form: | Oral Capsule, Extended Release |
Application #: | NDA012945 |
Rev. Date: |
Appearance:
Markings: | DIAMOX;754 |
Shapes: |
Capsule |
Colors: |
Orange |
Size (mm): | 23 |
Segments: * | 1 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines. |
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.
NDC Package Codes:
- 52125-070-02: 30 CAPSULE, EXTENDED RELEASE IN 1 BLISTER PACK (52125‑070‑02)
Active Ingredients:
- Acetazolamide
Dosage Strength:
- 500 mg
Inactive Ingredients:
- D&c Red No. 28
- D&c Yellow No. 10
- Fd&c Blue No. 1
- Fd&c Blue No. 2
- Fd&c Red No. 40
- Gelatin Hydrolysate (Porcine Skin, Mw 3000)
- Cellulose, Microcrystalline
- Propylene Glycol 1,2-distearate
- Sodium Lauryl Sulfate
- Ferrosoferric Oxide
- Talc
- Titanium Dioxide
Pharmaceutical Classes:
- Carbonic Anhydrase Inhibitor [EPC]
- Carbonic Anhydrase Inhibitors [MoA]
- Sulfonamides [Chemical/Ingredient]
Related Products:
Based on records with the same trade name.- 51285-754 Diamox 500 mg 12 Hr Extended Release Capsule by Duramed Pharmaceuticals, Inc.
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.