0615-8016 : Metoprolol Tartrate 50 mg Oral Tablet, Film Coated

NDC:	0615-8016
Labeler:	Ncs Healthcare of Ky, Inc Dba Vangard Labs
Product Type:	Human Prescription Drug
Drug Name:	Metoprolol Tartrate
Dosage Form:	Oral Tablet, Film Coated
Application #:	ANDA076704
Rev. Date:	Dec 23, 1993

Appearance:

Markings:	M;32
Shapes:	Round
Colors:	Pink
Size (mm):	8
Segments: ^*	2
^* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 2 indicates a scored pill which can be broken into 2 equal pieces.

M 32: (0378-0032) Metoprolol Tartrate 50 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:

0615-8016-05: 15 TABLET, FILM COATED IN 1 BLISTER PACK (0615‑8016‑05)
0615-8016-30: 6 BLISTER PACK IN 1 BOX, UNIT‑DOSE (0615‑8016‑30) > 5 TABLET, FILM COATED IN 1 BLISTER PACK
0615-8016-39: 30 TABLET, FILM COATED IN 1 BLISTER PACK (0615‑8016‑39)

Active Ingredients:

Metoprolol Tartrate

Dosage Strength:

50 mg

Inactive Ingredients:

Anhydrous Lactose
Silicon Dioxide
Croscarmellose Sodium
Hypromelloses
Magnesium Stearate
Cellulose, Microcrystalline
Polydextrose
Polyethylene Glycols
Povidone
Sodium Lauryl Sulfate
Titanium Dioxide
Triacetin
Fd&c Blue No. 2
D&c Red No. 27
Fd&c Red No. 40

Pharmaceutical Classes:

Adrenergic beta-Antagonists [MoA]
beta-Adrenergic Blocker [EPC]

NDC QR Code

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NDC 0615-8016 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.