NDC directory

Bremelanotide Acetate

Bremelanotide Acetate · Nanjing Hanxin Pharmaceutical Technology Co., Ltd. · POWDER

83821-206BULK INGREDIENTBulk ingredient
Product NDC
83821-206
Generic name
Bremelanotide Acetate
Labeler name
Nanjing Hanxin Pharmaceutical Technology Co., Ltd.
Finished
false
Listing expiration date
20271231
Marketing category
BULK INGREDIENT
Dosage form
POWDER
SPL ID
5cb63e2a-383d-8296-e063-6294a90ad869
Product type
BULK INGREDIENT
Marketing start date
20261001
Product ID
83821-206_5cb63e2a-383d-8296-e063-6294a90ad869
Active ingredients
  1. Name
    BREMELANOTIDE ACETATE
    Strength
    1 g/g
Packaging
  1. Package NDC
    83821-206-01
    Description
    1 g in 1 AMPULE (83821-206-01)
    Marketing start date
    01-OCT-26
  2. Package NDC
    83821-206-02
    Description
    1 g in 1 BAG (83821-206-02)
    Marketing start date
    01-OCT-26
  3. Package NDC
    83821-206-03
    Description
    5 g in 1 AMPULE (83821-206-03)
    Marketing start date
    01-OCT-26
  4. Package NDC
    83821-206-04
    Description
    5 g in 1 BAG (83821-206-04)
    Marketing start date
    01-OCT-26
  5. Package NDC
    83821-206-05
    Description
    10 g in 1 AMPULE (83821-206-05)
    Marketing start date
    01-OCT-26
  6. Package NDC
    83821-206-06
    Description
    10 g in 1 BAG (83821-206-06)
    Marketing start date
    01-OCT-26
  7. Package NDC
    83821-206-07
    Description
    20 g in 1 BAG (83821-206-07)
    Marketing start date
    01-OCT-26
  8. Package NDC
    83821-206-08
    Description
    50 g in 1 BAG (83821-206-08)
    Marketing start date
    01-OCT-26
  9. Package NDC
    83821-206-09
    Description
    100 g in 1 BAG (83821-206-09)
    Marketing start date
    01-OCT-26
  10. Package NDC
    83821-206-10
    Description
    200 g in 1 BAG (83821-206-10)
    Marketing start date
    01-OCT-26
  11. Package NDC
    83821-206-11
    Description
    500 g in 1 BAG (83821-206-11)
    Marketing start date
    01-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.