0904-5832 : Ranitidine 150 mg (As Ranitidine Hydrochloride 168 mg) Oral Tablet
| NDC: | 0904-5832 |
| Labeler: | Major Pharmaceuticals |
| Product Type: | Human OTC Drug |
| Drug Name: |  Major Ranitidine Maximum Strength |
| Dosage Form: | Oral Tablet |
| Application #: | ANDA078653 |
| Rev. Date: |
Appearance:
| Markings: | W;741 |
| Shapes: |
Hexagon (6 sides) |
| Colors: |
 Orange |
| Size (mm): | 11 |
| 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:
- 0904-5832-24: 3 BLISTER PACK IN 1 CARTON (0904‑5832‑24) > 8 TABLET IN 1 BLISTER PACK
- 0904-5832-51: 1 BOTTLE IN 1 CARTON (0904‑5832‑51) > 50 TABLET IN 1 BOTTLE
Active Ingredients:
- Ranitidine Hydrochloride
Dosage Strength:
- 150 mg
Inactive Ingredients:
- Silicon Dioxide
- Croscarmellose Sodium
- Diethyl Phthalate
- Fd&c Yellow No. 6
- Ferric Oxide Red
- Magnesium Stearate
- Cellulose, Microcrystalline
- Titanium Dioxide
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.