Guaifenesin 600 mg is a Oral Tablet, Extended Release in the Human Otc Drug category. It is labeled and distributed by Dr. Reddy's Laboratories Inc.. The primary component is Guaifenesin.
| Product ID | 43598-110_d04709e7-d5a7-3939-30fb-c2c2cfedc92f |
| NDC | 43598-110 |
| Product Type | Human Otc Drug |
| Proprietary Name | Guaifenesin 600 mg |
| Generic Name | Guaifenesin |
| Dosage Form | Tablet, Extended Release |
| Route of Administration | ORAL |
| Marketing Start Date | 2022-09-01 |
| Marketing Category | ANDA / |
| Application Number | ANDA215932 |
| Labeler Name | Dr. Reddy's Laboratories Inc. |
| Substance Name | GUAIFENESIN |
| Active Ingredient Strength | 600 mg/1 |
| Pharm Classes | Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |
| Marketing Start Date | 2022-09-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0363-0288 | childrens chest congestion | Guaifenesin |
| 0113-0325 | Good Sense Mucus ER | Guaifenesin |
| 0113-2023 | good sense mucus er | guaifenesin |
| 0113-3650 | Good Sense Mucus ER | Guaifenesin |
| 0113-0061 | good sense tussin | Guaifenesin |
| 0121-0744 | GUAIFENESIN | GUAIFENESIN |
| 0121-1488 | GUAIFENESIN | GUAIFENESIN |
| 0121-1744 | GUAIFENESIN | GUAIFENESIN |
| 0121-2232 | GUAIFENESIN | GUAIFENESIN |
| 0363-0028 | Guaifenesin | Guaifenesin |
| 0363-0033 | Guaifenesin | Guaifenesin |
| 0363-0071 | Mucus | Guaifenesin |
| 0363-0074 | Mucus | Guaifenesin |
| 0363-0532 | Mucus Relief | Guaifenesin |
| 0363-0325 | mucus relief er | Guaifenesin |
| 0031-9303 | Robitussin Direct Chest Congestion | guaifenesin |
| 0031-8724 | Robitussin Mucus Plus Chest Congestion | Guaifenesin |
| 0113-2061 | tussin | Guaifenesin |
| 0363-0310 | wal tussin | Guaifenesin |