0135-0057 : Sominex 25 mg Oral Tablet
NDC: | 0135-0057 |
Labeler: | Glaxosmithkline Consumer Healthcare Lp |
Product Type: | Human OTC Drug |
Drug Name: | Sominex |
Dosage Form: | Oral Tablet |
Application #: | part338 |
Rev. Date: |
Appearance:
Markings: | S |
Shapes: |
Round |
Colors: |
Blue |
Size (mm): | 10 |
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:
- 0135-0057-07: 16 TABLET IN 1 BLISTER PACK (0135‑0057‑07)
- 0135-0057-11: 32 TABLET IN 1 BLISTER PACK (0135‑0057‑11)
- 0135-0057-16: 72 TABLET IN 1 BLISTER PACK (0135‑0057‑16)
Active Ingredients:
- Diphenhydramine Hydrochloride
Dosage Strength:
- 25 mg
Inactive Ingredients:
- Calcium Phosphate, Dibasic, Dihydrate
- Fd&c Blue No. 1
- Aluminum Oxide
- Magnesium Stearate
- Cellulose, Microcrystalline
- Silicon Dioxide
- Starch, Corn
Related Products:
Based on records with the same trade name.- 0135-0058 Sominex Maximum Strength 50 mg Oral Tablet by Glaxosmithkline Consumer Healthcare Lp
- 63029-554 Sominex 25 mg Oral Tablet, Film Coated by Medtech Products Inc.
- 63029-555 Sominex 25 mg Oral Tablet by Medtech Products Inc.
- 67751-169 Sominex 25 mg Oral Tablet by Navajo Manufacturing Company Inc.
- 67751-221 Sominex 25 mg Oral Tablet, Film Coated by Navajo Manufacturing Company Inc.
NDC QR Code
Scan the QR code below to easily reference this data in the future:< Prev: 0135-0014Next: 0135-0058 >
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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.