NDC 70512-860 – Cabergoline

Cabergoline .5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70512-860

Product details

Brand name
Cabergoline
Generic name
Cabergoline
Labeler
SOLA Pharmaceuticals, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076310
Marketed since
May 8, 2023
Listing expires
December 31, 2026
Pharmacologic class
Ergot Derivative

Active ingredients

Uses, dosage, side effects and warnings for Cabergoline →

Package NDC codes (1)

Package NDCDescriptionSince
70512-860-088 TABLET in 1 BOTTLE (70512-860-08)May 8, 2023

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