NDC directory

Alprazolam

Unichem Pharmaceuticals (USA), Inc. · TABLET

29300-361ANDABenzodiazepine [EPC]
Product NDC
29300-361
Generic name
Alprazolam
Labeler name
Unichem Pharmaceuticals (USA), Inc.
Dea schedule
CIV
Brand name
Alprazolam
Finished
true
Listing expiration date
20271231
Marketing category
ANDA
Dosage form
TABLET
SPL ID
a806e27a-19e4-4780-b622-d9c9a062b37f
Product type
HUMAN PRESCRIPTION DRUG
Marketing start date
20261102
Product ID
29300-361_a806e27a-19e4-4780-b622-d9c9a062b37f
Application number
ANDA213204
Brand name base
Alprazolam
Active ingredients
  1. Name
    ALPRAZOLAM
    Strength
    .5 mg/1
Packaging
  1. Package NDC
    29300-361-01
    Description
    100 TABLET in 1 BOTTLE (29300-361-01)
    Marketing start date
    20261102
    Sample
    false
  2. Package NDC
    29300-361-05
    Description
    500 TABLET in 1 BOTTLE (29300-361-05)
    Marketing start date
    20261102
    Sample
    false
  3. Package NDC
    29300-361-10
    Description
    1000 TABLET in 1 BOTTLE (29300-361-10)
    Marketing start date
    20261102
    Sample
    false
Route
ORAL
Pharm class
Benzodiazepine [EPC], Benzodiazepines [CS]
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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.