Diclofenac Sodium

Product NDC: 63629-7069
11-digit product format: 636297069
Labeler code: 63629
Product ID: 63629-7069_37fd889d-3ffa-4368-b337-b20efb4e1fb0
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: diclofenac sodium
Dosage form: GEL
Route: TOPICAL
Labeler: Bryant Ranch Prepack
Application: NDA022122
Marketing category: NDA AUTHORIZED GENERIC
Marketing start: 2016-07-01
Marketing end: 0000-00-00
Substance: DICLOFENAC SODIUM
Active strength: 10 mg/g
Pharmacologic classes: Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag: No
Listing certified through: 2021-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
63629-7069-1	2020-10-16	C162847	48780-1	9d75b9cf-feba-f424-e053-dadaa90a57ce	cb227c0a-18aa-4a22-8e63-30f94746489e
63629-7069-1	2020-01-31	C162847	48780-1	9d75b9cf-feba-f424-e053-dadaa90a57ce	cb227c0a-18aa-4a22-8e63-30f94746489e

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
63629-7069-1	GM - Gram	63629-7069	c2cb5d0f-f2ae-4ce5-bc19-80d58fb30588	1	2018-05-09

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
QTG126297Q	DICLOFENAC SODIUM	15307-79-6	DICLOFENAC SODIUM

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63629-7069-1	63629706901	1 g in 1 BOTTLE (63629-7069-1)	1 g	2016-08-08	0000-00-00	No	No	Current