71610-556 : Metoprolol Tartrate 25 mg Oral Tablet, Film Coated

NDC:	71610-556
Labeler:	Aphena Pharma Solutions - Tennessee, LLC
Product Type:	Human Prescription Drug
Drug Name:	Metoprolol Tartrate
Dosage Form:	Oral Tablet, Film Coated
Application #:	ANDA076704
Rev. Date:	Jan 16, 2004

NDC Package Codes:

71610-556-30: 30 TABLET, FILM COATED IN 1 BOTTLE, PLASTIC (71610‑556‑30)
71610-556-45: 45 TABLET, FILM COATED IN 1 BOTTLE, PLASTIC (71610‑556‑45)
71610-556-53: 60 TABLET, FILM COATED IN 1 BOTTLE, PLASTIC (71610‑556‑53)
71610-556-60: 90 TABLET, FILM COATED IN 1 BOTTLE, PLASTIC (71610‑556‑60)
71610-556-70: 120 TABLET, FILM COATED IN 1 BOTTLE, PLASTIC (71610‑556‑70)
71610-556-80: 180 TABLET, FILM COATED IN 1 BOTTLE, PLASTIC (71610‑556‑80)
71610-556-92: 270 TABLET, FILM COATED IN 1 BOTTLE, PLASTIC (71610‑556‑92)
71610-556-98: 540 TABLET, FILM COATED IN 1 BOTTLE, PLASTIC (71610‑556‑98)

Active Ingredients:

Metoprolol Tartrate

Dosage Strength:

25 mg

Pharmaceutical Classes:

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

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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.