NDC 16714-621 – Zolpidem Tartrate

Zolpidem Tartrate 5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug DEA schedule CIV

Product NDC16714-621

Product details

Brand name
Zolpidem Tartrate
Generic name
Zolpidem Tartrate
Labeler
NorthStar Rx LLC
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 (3)

Package NDCDescriptionSince
16714-621-01100 TABLET, FILM COATED in 1 BOTTLE (16714-621-01)May 4, 2007
16714-621-02500 TABLET, FILM COATED in 1 BOTTLE (16714-621-02)May 4, 2007
16714-621-1110 BLISTER PACK in 1 CARTON (16714-621-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK (16714-621-10)May 4, 2007

Other zolpidem tartrate products