Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride is a Oral Tablet, Film Coated, Extended Release in the Human Otc Drug category. It is labeled and distributed by Sun Pharmaceutical Industries, Inc.. The primary component is Cetirizine Hydrochloride; Pseudoephedrine Hydrochloride.
| Product ID | 62756-915_69aa4eab-3b98-49a3-b0eb-d34411e61e0d |
| NDC | 62756-915 |
| Product Type | Human Otc Drug |
| Proprietary Name | Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride |
| Generic Name | Cetirizine Hydrochloride And Pseudoephedrine Hydrochloride |
| Dosage Form | Tablet, Film Coated, Extended Release |
| Route of Administration | ORAL |
| Marketing Start Date | 2012-09-29 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA090922 |
| Labeler Name | Sun Pharmaceutical Industries, Inc. |
| Substance Name | CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Active Ingredient Strength | 5 mg/1; mg/1 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2012-09-29 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA090922 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-09-29 |
| Marketing Category | ANDA |
| Application Number | ANDA090922 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-09-29 |
| Marketing Category | ANDA |
| Application Number | ANDA090922 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-09-29 |
| Marketing Category | ANDA |
| Application Number | ANDA090922 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2012-09-29 |
| Ingredient | Strength |
|---|---|
| CETIRIZINE HYDROCHLORIDE | 5 mg/1 |
| SPL SET ID: | 796c4b81-145b-4050-a851-dec81ff97006 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 45802-147 | Cetirizine hydrochloride and Pseudoephedrine hydrochloride | Cetirizine hydrochloride, Pseudoephedrine hydrochloride |
| 45802-721 | Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride | Cetirizine HCl, Pseudoephedrine HCl |
| 50090-1098 | Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride | Cetirizine HCl, Pseudoephedrine HCl |
| 62756-915 | Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride | Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride |
| 63187-955 | Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride | Cetirizine HCl, Pseudoephedrine HCl |
| 63868-964 | Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride | Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride |
| 68258-8907 | Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride | Cetirizine HCl, Pseudoephedrine HCl |
| 70677-0146 | all day allergy-D | Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride |
| 49035-982 | Allergy relief-D | Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride |
| 51660-940 | Allergy relief-D | Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride |
| 68016-531 | Allergy relief-D | Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride |
| 69842-994 | Allergy Relief-D | Cetirizine hydrochloride and pseudoephedrine hydrochloride |
| 70000-0163 | Allergy relief-D | Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride |
| 0363-0989 | Wal-Zyr D | Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride |
| 50580-728 | ZYRTEC-D | Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride |