FDA.reportPublic FDA data

62991-1513-6

Product NDC
62991-1513
Requested package NDC
62991-1513-6
11-digit product format
629911513
Labeler code
62991
Product ID
62991-1513_75781859-c422-4337-8d0f-d8461105caa2
Type
BULK INGREDIENT
Nonproprietary name
Apomorphine Hydrochloride
Dosage form
POWDER
Marketing category
BULK INGREDIENT
Marketing start
2010-10-27
Substance
APOMORPHINE HYDROCHLORIDE
Active strength
1 g/g
Listing certified through
2027-12-31
Current FDA listing
Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
unfinished packagepackage62991-151362991-1513-6UNFINISHEDActive or certified unfinished drug listing2026-10-15

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product
No
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
APOMORPHINE HYDROCHLORIDE1 g/g

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
62991-1513-1GM - Gram62991-1513c2d38402-7b14-4efb-8105-ac3804cdbbd712013-03-03
62991-1513-2GM - Gram62991-1513c1e1e291-1e95-47f9-b076-b4dbebff334c12013-03-03
62991-1513-3GM - Gram62991-1513ef63e51b-b36f-4ecf-a7f3-295403e6a30112013-03-03
62991-1513-4GM - Gram62991-1513537dff0f-b089-43c7-9b56-4456337f5bb712025-06-13

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startStatus
62991-1513-6629911513061000 g in 1 JAR (62991-1513-6)1000 g10-JUN-26Current