Altipres-B is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Alternative Pharmacal Corporation. The primary component is Brompheniramine Maleate; Dextromethorphan Hydrobromide; Phenylephrine Hydrochloride.
| Product ID | 53163-101_b6f67433-60ea-463d-944a-da069148fa64 |
| NDC | 53163-101 |
| Product Type | Human Otc Drug |
| Proprietary Name | Altipres-B |
| Generic Name | Brompheniramine Maleate, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride |
| Dosage Form | Liquid |
| Route of Administration | ORAL |
| Marketing Start Date | 2012-11-01 |
| Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
| Application Number | part341 |
| Labeler Name | Alternative Pharmacal Corporation |
| Substance Name | BROMPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Active Ingredient Strength | 4 mg/5mL; mg/5mL; mg/5mL |
| NDC Exclude Flag | N |
| Listing Certified Through | 2021-12-31 |
| Marketing Start Date | 2012-11-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC monograph final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-11-01 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| BROMPHENIRAMINE MALEATE | 4 mg/5mL |
| SPL SET ID: | fd00c41d-0580-4177-afaa-60bb12ca5a09 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 53163-101 | Altipres-B | BROMPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE |
| 45737-226 | Bio T Pres-B | BROMPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE |
| 0485-0204 | Rynex | Brompheniramine Maleate, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride |