NDC 65862-160 – Zolpidem Tartrate

Zolpidem Tartrate 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug DEA schedule CIV

Product NDC65862-160

Product details

Brand name
Zolpidem Tartrate
Generic name
Zolpidem Tartrate
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078413
Marketed since
May 4, 2007
Listing expires
December 31, 2026
Pharmacologic class
gamma-Aminobutyric Acid-ergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for Zolpidem tartrate →

Package NDC codes (4)

Package NDCDescriptionSince
65862-160-01100 TABLET, FILM COATED in 1 BOTTLE (65862-160-01)May 4, 2007
65862-160-05500 TABLET, FILM COATED in 1 BOTTLE (65862-160-05)May 4, 2007
65862-160-1010 BLISTER PACK in 1 CARTON (65862-160-10) / 10 TABLET, FILM COATED in 1 BLISTER PACKMay 4, 2007
65862-160-991000 TABLET, FILM COATED in 1 BOTTLE (65862-160-99)May 4, 2007

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