50090-2537 : Sunmark All Day Allergy D Oral Tablet, Extended Release
| NDC: | 50090-2537 |
| Labeler: | A-s Medication Solutions |
| Product Type: | Human OTC Drug |
| Drug Name: |  Sunmark All Day Allergy D |
| Dosage Form: | Oral Tablet, Extended Release |
| Application #: | ANDA077170 |
| Rev. Date: |
Appearance:
| Markings: | 5029;5;120 |
| Shapes: |
Round |
| Colors: |
 White |
| Size (mm): | 12 |
| 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. | |
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.
NDC Package Codes:
- 50090-2537-1: 4 BLISTER PACK IN 1 CARTON (50090‑2537‑1) > 6 TABLET, EXTENDED RELEASE IN 1 BLISTER PACK
Active Ingredients:
- Cetirizine Hydrochloride
- Pseudoephedrine Hydrochloride
Dosage Strength:
- 5 mg
- 120 mg
Inactive Ingredients:
- Silicon Dioxide
- Hypromellose, Unspecified
- Lactose Monohydrate
- Magnesium Stearate
- Microcrystalline Cellulose
- Talc
- Ferric Oxide Yellow /
Pharmaceutical Classes:
- Adrenergic alpha-Agonists [MoA]
- Histamine H1 Receptor Antagonists [MoA]
- Histamine-1 Receptor Antagonist [EPC]
- alpha-Adrenergic Agonist [EPC]
Related Products:
Based on records with the same trade name.- 49348-851 Cetirizine Dihydrochloride 5 mg / Pseudoephedrine Hydrochloride 120 mg 12 Hr Extended Release Tablet by Mckesson
- 70677-0077 Sunmark All Day Allergy D Oral Tablet, Film Coated, Extended Release by Strategic Sourcing Services LLC
NDC QR Code
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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.