Guaiatussin AC Sugar Free is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Hi-tech Pharmacal Co., Inc.. The primary component is Codeine Phosphate; Guaifenesin.
| Product ID | 50383-087_2b478682-1e0b-4664-86a2-1a039341cbd9 |
| NDC | 50383-087 |
| Product Type | Human Otc Drug |
| Proprietary Name | Guaiatussin AC Sugar Free |
| Generic Name | Guaifenesin And Codeine Phosphate |
| Dosage Form | Liquid |
| Route of Administration | ORAL |
| Marketing Start Date | 2010-09-08 |
| Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
| Application Number | part341 |
| Labeler Name | Hi-Tech Pharmacal Co., Inc. |
| Substance Name | CODEINE PHOSPHATE; GUAIFENESIN |
| Active Ingredient Strength | 10 mg/5mL; mg/5mL |
| DEA Schedule | CV |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2010-09-08 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC monograph final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2010-09-08 |
| Marketing Category | OTC monograph final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2010-09-08 |
| Marketing Category | OTC monograph final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2013-11-15 |
| Marketing Category | OTC monograph final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2010-09-08 |
| Marketing Category | OTC monograph final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2013-11-15 |
| Marketing Category | OTC monograph final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2010-09-08 |
| Ingredient | Strength |
|---|---|
| CODEINE PHOSPHATE | 10 mg/5mL |
| SPL SET ID: | b920eba2-27f2-402c-a7c9-d0988977965c |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 50090-2651 | Guaiatussin AC | guaifenesin and codeine phosphate |
| 50383-087 | Guaiatussin AC | guaifenesin and codeine phosphate |
| 68788-7550 | Guaiatussin AC | guaifenesin and codeine phosphate |
| 16571-302 | Guaifenesin AC | Guaifenesin and Codeine Phosphate |
| 0121-0775 | Guaifenesin and Codeine Phosphate | Guaifenesin and Codeine Phosphate |
| 0121-1550 | Guaifenesin and Codeine Phosphate | Guaifenesin and Codeine Phosphate |
| 0121-1775 | Guaifenesin and Codeine Phosphate | Guaifenesin and Codeine Phosphate |
| 12634-969 | Guaifenesin and Codeine Phosphate | Guaifenesin and Codeine Phosphate |
| 49999-610 | Guaifenesin and Codeine Phosphate | Guaifenesin and Codeine Phosphate |
| 50090-1428 | Guaifenesin and Codeine Phosphate | Guaifenesin and Codeine Phosphate |
| 53002-3191 | Guaifenesin and Codeine Phosphate | Guaifenesin and Codeine Phosphate |
| 61919-110 | GUAIFENESIN AND CODEINE PHOSPHATE | GUAIFENESIN AND CODEINE PHOSPHATE |
| 63187-117 | Guaifenesin and Codeine Phosphate | Guaifenesin and Codeine Phosphate |
| 68071-1350 | Guaifenesin and Codeine Phosphate | Guaifenesin and Codeine Phosphate |
| 68258-8904 | Guaifenesin and Codeine Phosphate | Guaifenesin and Codeine Phosphate |
| 68788-7608 | Guaifenesin and Codeine Phosphate | Guaifenesin and Codeine Phosphate |
| 70518-2434 | Guaifenesin and Codeine Phosphate | Guaifenesin and Codeine Phosphate |
| 70752-177 | GUAIFENESIN and CODEINE PHOSPHATE | GUAIFENESIN and CODEINE PHOSPHATE |
| 70752-180 | GUAIFENESIN and CODEINE PHOSPHATE | GUAIFENESIN and CODEINE PHOSPHATE |
| 0904-6479 | Robafen AC | Guaifenesin and Codeine Phosphate |