CHLORDIAZEPOXIDE

Product NDC: 61919-711
11-digit product format: 619190711
Labeler code: 61919
Product ID: 61919-711_2f1d49ad-13cc-2a23-e054-00144ff88e88
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: CHLORDIAZEPOXIDE
Dosage form: CAPSULE
Route: ORAL
Labeler: DIRECT RX
Application: ANDA085475
Marketing category: ANDA
Marketing start: 2016-03-04
Marketing end: 0000-00-00
Substance: CHLORDIAZEPOXID
Active strength: 25 mg/1
Pharmacologic classes: Benzodiazepine
DEA schedule: CIV
NDC exclude flag: E
Listing certified through: 2017-12-31
Current FDA listing: Historical FDA.report record