0078-0606 : Tekamlo 300/10 (Aliskiren / Amlodipine) Oral Tablet

NDC:	0078-0606
Labeler:	Novartis Pharmaceuticals Corporation
Product Type:	Human Prescription Drug
Drug Name:	Tekamlo
Dosage Form:	Oral Tablet, Film Coated
Application #:	NDA022545
Rev. Date:	Jan 1, 2010

Appearance:

Markings:	T12;NVR
Shapes:	Oval
Colors:	Brown
Size (mm):	21
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.

T12 NVR: (0078-0606) Tekamlo 300/10 (Aliskiren / Amlodipine) Oral Tablet by Novartis Pharmaceuticals Corporation

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:

0078-0606-15: 30 TABLET, FILM COATED IN 1 BOTTLE (0078‑0606‑15)
0078-0606-34: 90 TABLET, FILM COATED IN 1 BOTTLE (0078‑0606‑34)
0078-0606-35: 100 BLISTER PACK IN 1 PACKAGE (0078‑0606‑35) > 1 TABLET, FILM COATED IN 1 BLISTER PACK (0078‑0606‑61)

Active Ingredients:

Aliskiren Hemifumarate
Amlodipine Besylate

Dosage Strength:

300 mg
10 mg

Inactive Ingredients:

Silicon Dioxide
Crospovidone
Hypromelloses
Ferric Oxide Red
Ferric Oxide Yellow
Magnesium Stearate
Cellulose, Microcrystalline
Polyethylene Glycols
Povidones
Talc
Titanium Dioxide

Pharmaceutical Classes:

Renin Inhibitor [EPC]
Renin Inhibitors [MoA]
Calcium Channel Antagonists [MoA]
Dihydropyridine Calcium Channel Blocker [EPC]
Dihydropyridines [Chemical/Ingredient]

NDC QR Code

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NDC 0078-0606 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.