0085-0492 : Guanidine Hydrochloride 125 mg Oral Tablet
| NDC: | 0085-0492 |
| Labeler: | Merck Sharp & Dohme Corp. |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Guanidine Hydrochloride |
| Dosage Form: | Oral Tablet |
| Application #: | NDA001546 |
| Rev. Date: |
Appearance:
| Markings: | KEY;74 |
| Shapes: |
Round |
| Colors: |
 White |
| Size (mm): | 10 |
| 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:
- 0085-0492-01: 100 TABLET IN 1 BOTTLE (0085‑0492‑01)
Active Ingredients:
- Guanidine Hydrochloride
Dosage Strength:
- 125 mg
Inactive Ingredients:
- Silicon Dioxide
- Magnesium Stearate
- Mannitol
- Cellulose, Microcrystalline
Pharmaceutical Classes:
- Acetylcholine Releasing Agent [EPC]
- Increased Acetylcholine Activity [PE]
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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.