0615-7944 : Carvedilol 3.125 mg Oral Tablet, Film Coated

NDC:	0615-7944
Labeler:	Ncs Healthcare of Ky, Inc Dba Vangard Labs
Product Type:	Human Prescription Drug
Drug Name:	Carvedilol
Dosage Form:	Oral Tablet, Film Coated
Application #:	ANDA078332
Rev. Date:	Sep 5, 2007

Appearance:

Markings:	E;01
Shapes:	Oval
Colors:	White
Size (mm):	6
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.

E 01: (10544-184) Carvedilol 3.125 mg Oral Tablet, Film Coated by Ncs Healthcare of Ky, Inc Dba Vangard Labs

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:

0615-7944-30: 6 BLISTER PACK IN 1 BOX, UNIT‑DOSE (0615‑7944‑30) > 5 TABLET, FILM COATED IN 1 BLISTER PACK
0615-7944-39: 30 TABLET, FILM COATED IN 1 BLISTER PACK (0615‑7944‑39)

Active Ingredients:

Carvedilol

Dosage Strength:

3.125 mg

Inactive Ingredients:

Lactose Monohydrate
Silicon Dioxide
Crospovidone
Povidone K30
Sucrose
Magnesium Stearate
Polyethylene Glycol 400
Polysorbate 80
Titanium Dioxide
Hypromellose 2910 (5 Mpa.s)

Pharmaceutical Classes:

Adrenergic alpha-Antagonists [MoA]
Adrenergic beta1-Antagonists [MoA]
Adrenergic beta2-Antagonists [MoA]
alpha-Adrenergic Blocker [EPC]
beta-Adrenergic Blocker [EPC]

NDC QR Code

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NDC 0615-7944 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.