0615-7712 : Guaifenesin Extended Release 600 mg Oral Tablet, Extended Release
| NDC: | 0615-7712 |
| Labeler: | Ncs Healthcare of Ky, Inc Dba Vangard Labs |
| Product Type: | Human OTC Drug |
| Drug Name: |  Guaifenesin Extended Release Extended Release |
| Dosage Form: | Oral Tablet, Extended Release |
| Application #: | ANDA078912 |
| Rev. Date: |
Appearance:
| Markings: | L498 |
| Shapes: |
Round |
| Colors: |
 White |
| Size (mm): | 12 |
| 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:
- 0615-7712-39: 30 TABLET, EXTENDED RELEASE IN 1 BLISTER PACK (0615‑7712‑39)
Active Ingredients:
- Guaifenesin
Dosage Strength:
- 600 mg
Inactive Ingredients:
- Copovidone K25-31
- Silicon Dioxide
- Zinc Stearate
- Hydroxyethyl Cellulose (100 Mpa.s At 2%)
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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.