21695-820 : Fexofenadine Hydrochloride 60 mg / Pseudoephedrine Hydrochloride 120 mg 12 Hr Extended Release Tablet
| NDC: | 21695-820 |
| Labeler: | Rebel Distributors Corp |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride |
| Dosage Form: | Oral Tablet, Film Coated, Extended Release |
| Application #: | NDA020786 |
| Rev. Date: |
Appearance:
| Markings: | W07 |
| Shapes: |
Oval |
| Colors: |
 White |
| Size (mm): | 19 |
| 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. | |
NDC Package Codes:
- 21695-820-14: 14 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE (21695‑820‑14)
Active Ingredients:
- Fexofenadine Hydrochloride
- Pseudoephedrine Hydrochloride
Dosage Strength:
- 60 mg
- 120 mg
Inactive Ingredients:
- Cellulose, Microcrystalline
- Croscarmellose Sodium
- Magnesium Stearate
- Carnauba Wax
- Stearic Acid
- Silicon Dioxide
- Hypromelloses
- Polyethylene Glycol
Pharmaceutical Classes:
- Histamine H1 Receptor Antagonists [MoA]
- Histamine-1 Receptor Antagonist [EPC]
- Adrenergic alpha-Agonists [MoA]
- alpha-Adrenergic Agonist [EPC]
Related Products:
Based on records with the same trade name.- 0363-0044 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Extended Release by Walgreens Company
- 0363-0094 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Film Coated, Extended Release by Walgreen Co.
- 0363-2110 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Film Coated, Extended Release by Walgreens
- 0536-1384 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Extended Release by Rugby Laboratories
- 0536-1431 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Film Coated, Extended Release by Rugby Laboratories
- 0555-0725 Fexofenadine Hydrochloride 60 mg / Pseudoephedrine Hydrochloride 120 mg 12 Hr Extended Release Tablet by Barr Laboratories Inc.
- 11822-0021 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Extended Release by Rite Aid Corporation
- 30142-059 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Film Coated, Extended Release by Kroger Company
- 30142-097 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Extended Release by Kroger Company
- 37808-999 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Film Coated, Extended Release by H E B
- 41415-995 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Extended Release by Publix Super Markets, Inc
- 46122-452 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Film Coated, Extended Release by Amerisource Bergen
- 46122-694 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Film Coated, Extended Release by Amerisource Bergen
- 47335-724 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Film Coated, Extended Release by Sun Pharma Global Fze
- 51316-007 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Film Coated, Extended Release by Cvs Pharmacy, Inc.
- 51316-015 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Extended Release by Cvs Health Corp
- 51660-037 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Film Coated, Extended Release by Ohm Laboratories Inc.
- 54868-6087 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride (Fexofenadine Hydrochloride 60 mg / Pseudoephedrine Hydrochloride 120 mg) by Physicians Total Care, Inc.
- 56062-999 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Film Coated, Extended Release by Publix Super Markets Inc
- 58602-807 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Oral Tablet, Film Coated, Extended Release by Aurohealth LLC
- More related products ...
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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.