NDC 71205-060 – Naproxen

Naproxen 375 mg/1 · Tablet, Delayed Release · Oral

Human Prescription Drug

Product NDC71205-060

Product details

Brand name
Naproxen
Generic name
Naproxen
Labeler
Proficient Rx LP
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA091432
Marketed since
July 5, 2016
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Naproxen →

Package NDC codes (8)

Package NDCDescriptionSince
71205-060-1414 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-14)Jun 1, 2018
71205-060-1515 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-15)Jun 1, 2018
71205-060-2020 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-20)Jun 1, 2018
71205-060-3030 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-30)Jun 1, 2018
71205-060-4040 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-40)Jun 1, 2018
71205-060-4545 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-45)Jun 1, 2018
71205-060-6060 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-60)Jun 1, 2018
71205-060-9090 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-060-90)Jun 1, 2018

Other Naproxen products