63868-144 : Phenylephrine Hydrochloride 10 mg Oral Tablet
NDC: | 63868-144 |
Labeler: | Chain Drug Marketing Association Inc |
Product Type: | Human OTC Drug |
Drug Name: | Non-drowsy Maximum Strength Nasal Decongestant Pe |
Dosage Form: | Oral Tablet, Film Coated |
Application #: | part341 |
Rev. Date: |
Appearance:
Markings: | 44;453 |
Shapes: |
Round |
Colors: |
Red |
Size (mm): | 6 |
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:
- 63868-144-19: 1 BLISTER PACK IN 1 CARTON (63868‑144‑19) > 18 TABLET, FILM COATED IN 1 BLISTER PACK
- 63868-144-37: 2 BLISTER PACK IN 1 CARTON (63868‑144‑37) > 18 TABLET, FILM COATED IN 1 BLISTER PACK
- 63868-144-74: 4 BLISTER PACK IN 1 CARTON (63868‑144‑74) > 18 TABLET, FILM COATED IN 1 BLISTER PACK
Active Ingredients:
- Phenylephrine Hydrochloride
Dosage Strength:
- 10 mg
Inactive Ingredients:
- Croscarmellose Sodium
- Dextrose Monohydrate
- Calcium Phosphate, Dibasic, Dihydrate
- Fd&c Red No. 40
- Magnesium Stearate
- Maltodextrin
- Cellulose, Microcrystalline
- Carboxymethylcellulose Sodium
- Titanium Dioxide
Pharmaceutical Classes:
- Adrenergic alpha1-Agonists [MoA]
- alpha-1 Adrenergic Agonist [EPC]
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.