21695-043 : Nizatidine 300 mg Oral Capsule
NDC: | 21695-043 |
Labeler: | Rebel Distributors Corp |
Product Type: | Human Prescription Drug |
Drug Name: | Nizatidine |
Dosage Form: | Oral Capsule |
Application #: | ANDA075616 |
Rev. Date: |
Appearance:
Markings: | WPI;3138 |
Shapes: |
Capsule |
Colors: |
Brown |
Size (mm): | 22 |
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. |
NDC Package Codes:
- 21695-043-30: 30 CAPSULE IN 1 BOTTLE, PLASTIC (21695‑043‑30)
Active Ingredients:
- Nizatidine
Dosage Strength:
- 300 mg
Inactive Ingredients:
- Silicon Dioxide
- Starch, Corn
- Croscarmellose Sodium
- Magnesium Stearate
- Starch, Corn
- Ammonia
- Ferrosoferric Oxide
- Gelatin
- Potassium Hydroxide
- Propylene Glycol
- Shellac
- Sodium Lauryl Sulfate
- Titanium Dioxide
- Ferric Oxide Red
- Ferric Oxide Yellow
Pharmaceutical Classes:
- Histamine H2 Receptor Antagonists [MoA]
- Histamine-2 Receptor Antagonist [EPC]
Related Products:
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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.