OVIDE

Product NDC
51672-5276
11-digit product format
516725276
Labeler code
51672
Product ID
51672-5276_b25a87f3-4f04-4af3-8764-2cd11ef99913
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
MALATHION
Dosage form
LOTION
Route
TOPICAL
Labeler
TARO PHARMACEUTICALS USA, INC.
Application
NDA018613
Marketing category
NDA
Marketing start
1982-08-02
Marketing end
0000-00-00
Substance
MALATHION
Active strength
0 g/mL
Pharmacologic classes
Cholinesterase Inhibitors [MoA],Cholinesterase Inhibitor [EPC]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
51672-5276-4ML - Milliliter51672-5276a5ef88cf-9e56-43df-8636-27a03cf799a312012-07-24