NDC 0115-2622 – Terbutaline Sulfate

Terbutaline Sulfate 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC0115-2622

Product details

Brand name
Terbutaline Sulfate
Generic name
Terbutaline Sulfate
Labeler
Amneal Pharmaceuticals of New York LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA075877
Marketed since
June 26, 2001
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Terbutaline Sulfate →

Package NDC codes (2)

Package NDCDescriptionSince
0115-2622-01100 TABLET in 1 BOTTLE (0115-2622-01)Jun 26, 2001
0115-2622-02500 TABLET in 1 BOTTLE (0115-2622-02)Jun 26, 2001

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