0135-0148 : Tagamet Hb 200 mg Oral Tablet
NDC: | 0135-0148 |
Labeler: | Glaxosmithkline Consumer Healthcare Lp |
Product Type: | Human OTC Drug |
Drug Name: | ![]() |
Dosage Form: | Oral Tablet |
Application #: | NDA020238 |
Rev. Date: |
Appearance:
Markings: | TAGAMET;200 |
Shapes: |
Diamond (4 sides) |
Colors: |
![]() |
Size (mm): | 13 |
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:
- 0135-0148-02: 6 TABLET IN 1 BLISTER PACK (0135‑0148‑02)
- 0135-0148-05: 30 TABLET IN 1 BLISTER PACK (0135‑0148‑05)
Active Ingredients:
- Cimetidine
Dosage Strength:
- 200 mg
Inactive Ingredients:
- Powdered Cellulose
- Starch, Corn
- Hypromelloses
- Magnesium Stearate
- Polyethylene Glycols
- Polysorbate 80
- Povidones
- Sodium Lauryl Sulfate
- Sodium Starch Glycolate Type a Potato
- Titanium Dioxide
Related Products:
Based on records with the same trade name.- 52183-223 Tagamet 200 mg Oral Tablet by Prestige Brands Holdings, Inc.
- 63029-222 Tagamet Hb 200 mg Oral Tablet by Medtech Products Inc.
- 63029-223 Tagamet 200 mg Oral Tablet by Medtech Products Inc.
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.