51862-896 : Tilia FeTilia Fe Kit


NDC51862-896
Labeler: Mayne Pharma Inc.
Product Type: Human Prescription Drug
Drug Name:  Tilia Fe
Dosage Form: Kit
Application #: ANDA202962
Rev. Date: 


NDC Package Codes:

  • 51862-896-01: 1 BLISTER PACK IN 1 PACKET (51862‑896‑01) > 1 KIT IN 1 BLISTER PACK
  • 51862-896-02: 1 BLISTER PACK IN 1 CARTON (51862‑896‑02) > 1 KIT IN 1 BLISTER PACK
  • 51862-896-03: 3 BLISTER PACK IN 1 CARTON (51862‑896‑03) > 1 KIT IN 1 BLISTER PACK
  • 51862-896-06: 6 BLISTER PACK IN 1 CARTON (51862‑896‑06) > 1 KIT IN 1 BLISTER PACK

Related Products:

Based on records with the same trade name.
  • 51862-284 Tilia Fe Oral Kit by Mayne Pharma Inc.
  • 21695-685 Tilia Fe 28 Day Pack by Rebel Distributors Corp
  • 52544-054 Tilia Fe Oral Kit by Actavis Pharma, Inc.
  • 52544-143 Tilia Fe 28 Day Pack by Watson Pharma, Inc.
  • 52544-175 Tilia Fe 28 Day Pack by Watson Pharma, Inc.
  • 54868-6274 Tilia Fe 28 Day Pack by Physicians Total Care, Inc.
  • 75907-086 Tilia FeTilia Fe Kit by Dr. Reddy’s Laboratories Inc.

NDC QR Code

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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.