NDC 0046-1100 – Premarin

Estrogens, Conjugated .3 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC0046-1100

Product details

Brand name
Premarin
Generic name
estrogens, conjugated
Labeler
Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA004782
Marketed since
January 1, 2006
Listing expires
December 31, 2027
Pharmacologic class
Estrogen

Active ingredients

Uses, dosage, side effects and warnings for Premarin →

Package NDC codes (3)

Package NDCDescriptionSince
0046-1100-521 BLISTER PACK in 1 CARTON (0046-1100-52) / 5 TABLET, FILM COATED in 1 BLISTER PACKNov 11, 2019
0046-1100-81100 TABLET, FILM COATED in 1 BOTTLE (0046-1100-81)Jan 1, 2006
0046-1100-911 BOTTLE in 1 CARTON (0046-1100-91) / 1000 TABLET, FILM COATED in 1 BOTTLEJan 1, 2006

Recalls mentioning this NDC

Other Premarin products