0074-3287 : Tarka 2/180 24 Hr Extended Release Tablet
| NDC: | 0074-3287 |
| Labeler: | Abbvie Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Tarka |
| Dosage Form: | Oral Tablet, Film Coated, Extended Release |
| Application #: | NDA020591 |
| Rev. Date: |
Appearance:
| Markings: | 182 |
| Shapes: |
Oval |
| Colors: |
 Pink |
| Size (mm): | 18 |
| 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:
- 0074-3287-13: 100 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE (0074‑3287‑13)
Active Ingredients:
- Trandolapril
- Verapamil Hydrochloride
Dosage Strength:
- 2 mg
- 180 mg
Inactive Ingredients:
- Docusate Sodium
- Alcohol
- Magnesium Stearate
- Cellulose, Microcrystalline
- Water
- Silicon Dioxide
- Sodium Alginate
- Sodium Stearyl Fumarate
- Talc
- Titanium Dioxide
- Starch, Corn
- Hypromelloses
- Polyethylene Glycols
- Lactose Monohydrate
- Hydroxypropyl Cellulose (Type H)
- Povidones
- Ferric Oxide Red
Pharmaceutical Classes:
- Angiotensin Converting Enzyme Inhibitor [EPC]
- Angiotensin-converting Enzyme Inhibitors [MoA]
- Calcium Channel Antagonists [MoA]
- Calcium Channel Blocker [EPC]
- Cytochrome P450 3A4 Inhibitors [MoA]
- Cytochrome P450 3A Inhibitors [MoA]
- P-Glycoprotein Inhibitors [MoA]
Related Products:
Based on records with the same trade name.- 0074-3288 Tarka 1/240 24 Hr Extended Release Tablet by Abbvie Inc.
- 0074-3289 Tarka 2/240 24 Hr Extended Release Tablet by Abbvie Inc.
- 0074-3290 Tarka 4/240 24 Hr Extended Release Tablet by Abbvie Inc.
- 54868-5311 Tarka 2/240 24 Hr Extended Release Tablet by Physicians Total Care, Inc.
- 54868-5320 Tarka 4/240 24 Hr Extended Release Tablet by Physicians Total Care, Inc.
- 54868-5548 Tarka 2/180 24 Hr Extended Release Tablet by Physicians Total Care, 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.