Naproxen

Product NDC
70868-200
11-digit product format
708680200
Labeler code
70868
Product ID
70868-200_ee815be2-8c61-41de-8397-72a0d1908be5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Naproxen
Dosage form
SUSPENSION
Route
ORAL
Labeler
Key Therapeutics, LLC
Application
NDA018965
Marketing category
NDA
Marketing start
2016-11-11
Marketing end
0000-00-00
Substance
NAPROXEN
Active strength
125 mg/5mL
Pharmacologic classes
Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
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
70868-200-16ML - Milliliter70868-2005c4f5123-4f43-4164-9358-96820edc522712016-12-07