Home NDC 0003-1965 ZERIT
Product NDC 0003-1965
11-digit product format 000031965
Labeler code 0003
Product ID 0003-1965_41d3b607-aa70-408b-9e05-c3e285482568
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name stavudine
Dosage form CAPSULE, GELATIN COATED
Route ORAL
Labeler E.R. Squibb & Sons, L.L.C.
Application NDA020412
Marketing category NDA
Marketing start 1994-06-24
Marketing end 2020-08-31
Substance STAVUDINE
Active strength 20 mg/1
Pharmacologic classes Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [EXT],Nucleoside Reverse Transcriptase Inhibitors [MoA]
NDC exclude flag No
Listing certified through 0000-00-00
Current FDA listing Historical FDA.report record DailyMed Product Concepts# DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded STAVUDINE ACTIVE INGREDIENT BO9LE4QFZF ZERIT (STAVUDINE) CAPSULE, GELATIN COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY] 3 stavudine ACTIVE MOIETY BO9LE4QFZF ZERIT (STAVUDINE) CAPSULE, GELATIN COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY] 3 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U ZERIT (STAVUDINE) CAPSULE, GELATIN COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY] 3 GELATIN INACTIVE INGREDIENT 2G86QN327L ZERIT (STAVUDINE) CAPSULE, GELATIN COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY] 3 LACTOSE INACTIVE INGREDIENT J2B2A4N98G ZERIT (STAVUDINE) CAPSULE, GELATIN COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY] 3 MAGNESIUM STEARATE INACTIVE INGREDIENT 70097M6I30 ZERIT (STAVUDINE) CAPSULE, GELATIN COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY] 3 SODIUM STARCH GLYCOLATE TYPE A POTATO INACTIVE INGREDIENT 5856J3G2A2 ZERIT (STAVUDINE) CAPSULE, GELATIN COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY] 3 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP ZERIT (STAVUDINE) CAPSULE, GELATIN COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY] 3
DailyMed RxNorm Mappings#