Pregabalin

Product NDC: 72606-008
11-digit product format: 726060008
Labeler code: 72606
Product ID: 72606-008_f52fb718-9ad9-4e60-aec5-bbb97fe81a83
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: pregabalin
Dosage form: CAPSULE
Route: ORAL
Labeler: CELLTRION USA, INC.
Application: ANDA212865
Marketing category: ANDA
Marketing start: 2020-03-31
Marketing end: 0000-00-00
Substance: PREGABALIN
Active strength: 150 mg/1
DEA schedule: CV
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
72606-008-01	2025-03-14	C162847	48780-1	1030e364-fff0-111a-e063-dadaa90a10e2	031f843b-9251-49c7-b2e7-be4cbd2e2295
72606-008-01	2024-01-30	C162847	48780-1	1030e364-fff0-111a-e063-dadaa90a10e2	031f843b-9251-49c7-b2e7-be4cbd2e2295

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
72606-008-01	EA - Each	72606-008	124364df-e9b9-4344-9a3c-780512553dd1	1	2020-07-13

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
72606-008-01	72606000801	90 CAPSULE in 1 BOTTLE (72606-008-01)	90 capsule	2020-03-31	0000-00-00	No	No	Current