49349-229 : Hydralazine Hydrochloride 25 mg Oral Tablet
NDC: | 49349-229 |
Labeler: | Remedyrepack Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | Hydralazine Hydrochloride |
Dosage Form: | Oral Tablet, Film Coated |
Application #: | ANDA086242 |
Rev. Date: |
Appearance:
Markings: | HP;2 |
Shapes: |
Round |
Colors: |
Pink |
Size (mm): | 8 |
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:
- 49349-229-02: 30 TABLET, FILM COATED IN 1 BLISTER PACK (49349‑229‑02)
Active Ingredients:
- Hydralazine Hydrochloride
Dosage Strength:
- 25 mg
Inactive Ingredients:
- Fd&c Red No. 40
- Hypromelloses
- Anhydrous Lactose
- Mineral Oil
- Cellulose, Microcrystalline
- Magnesium Stearate
- Starch, Corn
- Sodium Lauryl Sulfate
- Titanium Dioxide
Pharmaceutical Classes:
- Arteriolar Vasodilation [PE]
- Arteriolar Vasodilator [EPC]
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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.