DailyMed label

minocycline hydrochloride

DailyMed label · Zydus Lifesciences Limited · version 4

Key facts

Product minocycline hydrochloride
Labeler Zydus Lifesciences Limited
Document type HUMAN PRESCRIPTION DRUG LABEL
Active ingredients MINOCYCLINE HYDROCHLORIDE
Active ingredient UNIIs 0020414E5U
Application number 203553
Route ORAL
NDC package codes 70771-1138-3, 70771-1138-9, 70771-1138-1, 70771-1138-5, 70771-1138-0, 70771-1138-7, 70771-1153-3, 70771-1153-9, 70771-1153-1, 70771-1153-5, 70771-1153-0, 70771-1153-7 and 36 more
Effective date Jun 5, 2025
Set ID 8bf9cf23-8ffc-401f-981d-4878d694a468

At a glance

  • 10–99 NDC package codes
  • 1–9 Active ingredients
  • None 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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