Oseltamivir Phosphate

Product NDC: 63739-038
11-digit product format: 637390038
Labeler code: 63739
Product ID: 63739-038_f45785e4-a8ba-4b30-b257-126860df1d06
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Oseltamivir phosphate
Dosage form: CAPSULE
Route: ORAL
Labeler: McKesson Corporation dba SKY Packaging
Application: ANDA202595
Marketing category: ANDA
Marketing start: 2016-12-12
Marketing end: 0000-00-00
Substance: OSELTAMIVIR PHOSPHATE
Active strength: 30 mg/1
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
63739-038-07	2020-07-22	C162847	48780-1	ab0e2407-26e1-f274-e053-dbdaa90a6471	216ec984-90a9-4b81-aa07-eb7f7cd2f5f3

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
63739-038-07	EA - Each	63739-038	b94bfa74-5c87-4590-b4d1-3246d2d08102	1	2017-12-14

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63739-038-07	63739003807	1 BLISTER PACK in 1 CARTON (63739-038-07) > 10 CAPSULE in 1 BLISTER PACK	1 blister pack	2017-11-01	0000-00-00	No	No	Current