Naproxen sodium

Product NDC
69230-313
11-digit product format
692300313
Labeler code
69230
Product ID
69230-313_812f4f85-2d79-4827-a2b9-4905b0f02ff1
Type
HUMAN OTC DRUG
Nonproprietary name
Naproxen sodium
Dosage form
TABLET
Route
ORAL
Labeler
Camber Consumer Care
Application
ANDA207612
Marketing category
ANDA
Marketing start
2019-12-11
Marketing end
0000-00-00
Substance
NAPROXEN SODIUM
Active strength
220 mg/1
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fef6ad89-235f-4274-ba49-a8e53642473eProduct name220250225
87fed3e6-8fba-48ef-96b0-3a7fb54b96ffProduct name320230306
b5fdaaec-7251-4da6-9cb2-4e9e76939ec8Product name120200623
e76dbbc1-775d-722c-08ff-ed45e8a80defProduct name320181002
6f4f4521-fd56-1ae6-888b-3b021bd75c7cProduct name120140508
ce67e27d-1d21-5465-4409-b0662dd99d4dProduct name120140508

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
69230-313-01EA - Each69230-31327e100b0-a445-4634-866f-27891720c98c12020-07-13
69230-313-05EA - Each69230-31353a37cf2-f0c9-43ad-8f86-58594b00844b12020-07-13
69230-313-50EA - Each69230-31347ad2e17-15fc-4c3e-9ec2-a6c0a2233c9912020-07-13

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
849574naproxen sodium 220 MG Oral TabletPSN9e9dc1fb-aa0f-4948-b4aa-75a94f9f9d573
849574naproxen sodium 220 MG Oral TabletSCD9e9dc1fb-aa0f-4948-b4aa-75a94f9f9d573
849574naproxen sodium 220 MG (as naproxen 200 MG) Oral TabletSY9e9dc1fb-aa0f-4948-b4aa-75a94f9f9d573