Emcyt

Product NDC
0013-0132
11-digit product format
000130132
Labeler code
0013
Product ID
0013-0132_33a0b2e3-316f-42e5-979e-aad10c550611
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
estramustine phosphate sodium
Dosage form
CAPSULE
Route
ORAL
Labeler
Pharmacia and Upjohn Company LLC
Application
NDA018045
Marketing category
NDA
Marketing start
1992-01-01
Marketing end
0000-00-00
Substance
ESTRAMUSTINE PHOSPHATE SODIUM
Active strength
140 mg/1
Pharmacologic classes
Alkylating Activity [MoA],Alkylating Drug [EPC],Estradiol [CS],Nitrogen Mustard Compounds [CS]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0013-0132-02EA - Each0013-013268e595c0-8b9a-4ef6-9113-5d6b5c98363812012-07-24

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0013-0132-02000130132021 BOTTLE in 1 CARTON (0013-0132-02) > 100 CAPSULE in 1 BOTTLE1 bottle1992-01-010000-00-00NoNoCurrent