TRUSOPT

Product NDC: 0006-3519
11-digit product format: 000063519
Labeler code: 0006
Product ID: 0006-3519_1482d00e-8ed4-496b-be57-9a22b09139bd
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: dorzolamide hydrochloride
Dosage form: SOLUTION
Route: OPHTHALMIC
Labeler: Merck Sharp & Dohme LLC
Application: NDA020408
Marketing category: NDA
Marketing start: 1994-12-09
Marketing end: 0000-00-00
Substance: DORZOLAMIDE HYDROCHLORIDE
Active strength: 20 mg/mL
Pharmacologic classes: Carbonic Anhydrase Inhibitor [EPC], Carbonic Anhydrase Inhibitors [MoA]
NDC exclude flag: No
Listing certified through: 2023-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
0006-3519-36	2021-01-20	C162847	48780-1	9d75b9d0-9934-f424-e053-dadaa90a57ce	26d26f80-aebf-441c-6383-327cb95eae4d
0006-3519-36	2020-01-31	C162847	48780-1	9d75b9d0-9934-f424-e053-dadaa90a57ce	26d26f80-aebf-441c-6383-327cb95eae4d

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0006-3519-36	ML - Milliliter	0006-3519	4d2d892f-c6f7-4cea-afdc-f58fa04b3978	1	2012-07-24

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
QZO5366EW7	DORZOLAMIDE HYDROCHLORIDE	130693-82-2	DORZOLAMIDE HYDROCHLORIDE

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
0006-3519-36	00006351936	1 BOTTLE, DROPPER in 1 CARTON (0006-3519-36) > 10 mL in 1 BOTTLE, DROPPER	1994-12-09	0000-00-00	No	No	Current