NDC directory

Semaglutide

Semaglutide · SHILPA PHARMA LIFESCIENCES LIMITED · POWDER

82920-505BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDINGBulk ingredient
Product NDC
82920-505
Generic name
Semaglutide
Labeler name
SHILPA PHARMA LIFESCIENCES LIMITED
Finished
false
Listing expiration date
20271231
Marketing category
BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Dosage form
POWDER
SPL ID
508db265-e9a5-d852-e063-6294a90a7d07
Product type
BULK INGREDIENT
Marketing start date
20260430
Product ID
82920-505_508db265-e9a5-d852-e063-6294a90a7d07
Active ingredients
  1. Name
    SEMAGLUTIDE
    Strength
    1 g/g
Packaging
  1. Package NDC
    82920-505-01
    Description
    10 BOTTLE in 1 CONTAINER (82920-505-01) / 25 g in 1 BOTTLE
    Marketing start date
    30-APR-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.