DailyMed label

BROMOCRIPTINE MESYLATE

DailyMed label · Sun Pharmaceutical Industries, Inc. · version 4

Key facts

Product BROMOCRIPTINE MESYLATE
Labeler Sun Pharmaceutical Industries, Inc.
Document type HUMAN PRESCRIPTION DRUG LABEL
Active ingredients BROMOCRIPTINE MESYLATE
Active ingredient UNIIs FFP983J3OD
Application number 017962
Route ORAL
NDC package codes 63304-962-01, 63304-962-30, 63304-158-01, 63304-158-30
Effective date Feb 6, 2020
Set ID 44cc1e5f-c509-40e6-ac51-eba6d0440b16

At a glance

  • 1–9 NDC package codes
  • 1–9 Active ingredients
  • 1–9 Manufacturing establishments listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About DailyMed drug labels

DailyMed publishes the structured product labeling (SPL) that companies submit to the FDA, including package NDCs, ingredients and the establishments that make each product.

Source: U.S. National Library of Medicine (NLM), DailyMed · Source date:

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