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"51991-704-10" National Drug Code (NDC)
Alprazolam 1000 TABLET in 1 BOTTLE (51991-704-10)
(Breckenridge Pharmaceutical, Inc.)
NDC Code
51991-704-10
Package Description
1000 TABLET in 1 BOTTLE (51991-704-10)
Product NDC
51991-704
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Alprazolam
Non-Proprietary Name
Alprazolam
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20180709
End Marketing Date
20251031
Marketing Category Name
ANDA
Application Number
ANDA207507
Manufacturer
Breckenridge Pharmaceutical, Inc.
Substance Name
ALPRAZOLAM
Strength
.25
Strength Unit
mg/1
Pharmacy Classes
Benzodiazepine [EPC], Benzodiazepines [CS]
DEA Schedule
CIV
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51991-704-10