NDC directory

epinephrine

Gland Pharma Limited · INJECTION

68083-701ANDAAdrenergic alpha-Agonists [MoA]
Product NDC
68083-701
Generic name
epinephrine
Labeler name
Gland Pharma Limited
Brand name
epinephrine
Finished
true
Listing expiration date
20271231
Marketing category
ANDA
Dosage form
INJECTION
SPL ID
cff9d22e-947e-497f-a58b-635e55434623
Product type
HUMAN PRESCRIPTION DRUG
Marketing start date
20261026
Product ID
68083-701_cff9d22e-947e-497f-a58b-635e55434623
Application number
ANDA220400
Brand name base
epinephrine
Active ingredients
  1. Name
    EPINEPHRINE
    Strength
    1 mg/mL
Packaging
  1. Package NDC
    68083-701-01
    Description
    1 VIAL in 1 CARTON (68083-701-01) / 30 mL in 1 VIAL
    Marketing start date
    20261026
    Sample
    false
Route
INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Pharm class
Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Catecholamine [EPC], Catecholamines [CS], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC]
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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.