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FDA updates labeling for MEPERIDINE HYDROCHLORIDE PRESERVATIVE FREE

  • FDA Approval
  • Dec. 31, 2025, 13:45 UTC
  • 7
  • 0 comments

Labeling changes approved for WEST-WARD PHARMS INT. Active ingredient: MEPERIDINE HYDROCHLORIDE. Decision date: 12/22/2025

Comment Full text

FDA updates labeling for ACETAMINOPHEN AND CODEINE PHOSPHATE

  • FDA Approval
  • Dec. 31, 2025, 13:45 UTC
  • 9
  • 0 comments

Labeling changes approved for FOSUN PHARMA. Active ingredient: ACETAMINOPHEN; CODEINE PHOSPHATE. Decision date: 12/22/2025

Comment Full text

FDA updates labeling for ACETAMINOPHEN AND CODEINE PHOSPHATE

  • FDA Approval
  • Dec. 31, 2025, 13:45 UTC
  • 8
  • 0 comments

Labeling changes approved for FOSUN PHARMA. Active ingredient: ACETAMINOPHEN; CODEINE PHOSPHATE. Decision date: 12/22/2025

Comment Full text

FDA updates labeling for NALBUPHINE HYDROCHLORIDE

  • FDA Approval
  • Dec. 31, 2025, 13:45 UTC
  • 9
  • 0 comments

Labeling changes approved for HOSPIRA. Active ingredient: NALBUPHINE HYDROCHLORIDE. Decision date: 12/22/2025

Comment Full text

FDA updates labeling for MEPERIDINE HYDROCHLORIDE

  • FDA Approval
  • Dec. 31, 2025, 13:45 UTC
  • 7
  • 0 comments

Labeling changes approved for BARR. Active ingredient: MEPERIDINE HYDROCHLORIDE. Decision date: 12/22/2025

Comment Full text

FDA updates labeling for ACETAMINOPHEN AND CODEINE PHOSPHATE

  • FDA Approval
  • Dec. 31, 2025, 13:45 UTC
  • 13
  • 0 comments

Labeling changes approved for STRIDES PHARMA INTL. Active ingredient: ACETAMINOPHEN; CODEINE PHOSPHATE. Decision date: 12/22/2025

Comment Full text

FDA updates labeling for ACETAMINOPHEN AND CODEINE PHOSPHATE

  • FDA Approval
  • Dec. 31, 2025, 13:45 UTC
  • 11
  • 0 comments

Labeling changes approved for STRIDES PHARMA INTL. Active ingredient: ACETAMINOPHEN; CODEINE PHOSPHATE. Decision date: 12/22/2025

Comment Full text

FDA updates labeling for NALBUPHINE HYDROCHLORIDE

  • FDA Approval
  • Dec. 31, 2025, 13:45 UTC
  • 7
  • 0 comments

Labeling changes approved for DR REDDYS. Active ingredient: NALBUPHINE HYDROCHLORIDE. Decision date: 12/22/2025

Comment Full text

FDA updates labeling for BUTORPHANOL TARTRATE

  • FDA Approval
  • Dec. 31, 2025, 13:45 UTC
  • 11
  • 0 comments

Labeling changes approved for HIKMA FARMACEUTICA. Active ingredient: BUTORPHANOL TARTRATE. Decision date: 12/22/2025

Comment Full text

FDA updates labeling for BUPRENORPHINE HYDROCHLORIDE

  • FDA Approval
  • Dec. 31, 2025, 13:45 UTC
  • 6
  • 0 comments

Labeling changes approved for HIKMA. Active ingredient: BUPRENORPHINE HYDROCHLORIDE. Decision date: 12/22/2025

Comment Full text
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