NDC directory

Semaglutide

Semaglutide · Hybio Pharmaceutical Co., Ltd. · POWDER

14403-0030BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDINGBulk ingredient
Product NDC
14403-0030
Generic name
Semaglutide
Labeler name
Hybio Pharmaceutical Co., Ltd.
Finished
false
Listing expiration date
20271231
Marketing category
BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Dosage form
POWDER
SPL ID
5df38409-66bb-ad87-e063-6394a90aaa73
Product type
BULK INGREDIENT
Marketing start date
20261016
Product ID
14403-0030_5df38409-66bb-ad87-e063-6394a90aaa73
Active ingredients
  1. Name
    SEMAGLUTIDE
    Strength
    1 g/g
Packaging
  1. Package NDC
    14403-0030-2
    Description
    1 BOTTLE in 1 BAG (14403-0030-2) / 10 g in 1 BOTTLE
    Marketing start date
    16-OCT-26
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.