NDC 70771-1476 – Tadalafil

Tadalafil 5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70771-1476

Product details

Brand name
Tadalafil
Generic name
Tadalafil
Labeler
Zydus Lifesciences Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA206693
Marketed since
March 27, 2019
Listing expires
December 31, 2026
Pharmacologic class
Phosphodiesterase 5 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Tadalafil →

Package NDC codes (7)

Package NDCDescriptionSince
70771-1476-01000 TABLET, FILM COATED in 1 BOTTLE (70771-1476-0)Mar 27, 2019
70771-1476-1100 TABLET, FILM COATED in 1 BOTTLE (70771-1476-1)Mar 27, 2019
70771-1476-330 TABLET, FILM COATED in 1 BOTTLE (70771-1476-3)Mar 27, 2019
70771-1476-42 BLISTER PACK in 1 CARTON (70771-1476-4) / 15 TABLET, FILM COATED in 1 BLISTER PACKMar 27, 2019
70771-1476-5500 TABLET, FILM COATED in 1 BOTTLE (70771-1476-5)Mar 27, 2019
70771-1476-710 TABLET, FILM COATED in 1 BOTTLE (70771-1476-7)Mar 27, 2019
70771-1476-990 TABLET, FILM COATED in 1 BOTTLE (70771-1476-9)Mar 27, 2019

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