NDC directory

Semaglutide

Semaglutide · Fujian Genohope Biotech Ltd. · POWDER

84502-113BULK INGREDIENTBulk ingredient
Product NDC
84502-113
Generic name
Semaglutide
Labeler name
Fujian Genohope Biotech Ltd.
Finished
false
Listing expiration date
20271231
Marketing category
BULK INGREDIENT
Dosage form
POWDER
SPL ID
53bee5f1-3391-1231-e063-6394a90a9894
Product type
BULK INGREDIENT
Marketing start date
20260519
Product ID
84502-113_53bee5f1-3391-1231-e063-6394a90a9894
Active ingredients
  1. Name
    SEMAGLUTIDE
    Strength
    1 g/g
Packaging
  1. Package NDC
    84502-113-01
    Description
    500 g in 1 BAG (84502-113-01)
    Marketing start date
    19-MAY-26
  2. Package NDC
    84502-113-02
    Description
    1000 g in 1 BAG (84502-113-02)
    Marketing start date
    19-MAY-26
  3. Package NDC
    84502-113-03
    Description
    10 g in 1 BOTTLE (84502-113-03)
    Marketing start date
    19-MAY-26
  4. Package NDC
    84502-113-04
    Description
    50 g in 1 BOTTLE (84502-113-04)
    Marketing start date
    19-MAY-26
  5. Package NDC
    84502-113-05
    Description
    100 g in 1 BOTTLE (84502-113-05)
    Marketing start date
    19-MAY-26
  6. Package NDC
    84502-113-06
    Description
    5 g in 1 TUBE (84502-113-06)
    Marketing start date
    19-MAY-26
  7. Package NDC
    84502-113-07
    Description
    1 g in 1 TUBE (84502-113-07)
    Marketing start date
    19-MAY-26
  8. Package NDC
    84502-113-08
    Description
    25 g in 1 BOTTLE (84502-113-08)
    Marketing start date
    19-MAY-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.