Megestrol Acetate

Product NDC: 63739-165
11-digit product format: 637390165
Labeler code: 63739
Product ID: 63739-165_b3d6e73b-1fc1-4e7f-e053-2a95a90ac1e7
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Megestrol Acetate
Dosage form: TABLET
Route: ORAL
Labeler: McKesson Corporation dba SKY Packaging
Application: ANDA072423
Marketing category: ANDA
Marketing start: 1988-08-08
Marketing end: 2021-07-31
Substance: MEGESTROL ACETATE
Active strength: 40 mg/1
Pharmacologic classes: Progesterone Congeners [CS],Progestin [EPC]
NDC exclude flag: No
Listing certified through: 0000-00-00
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
63739-165-10	2020-07-22	C162847	48780-1	ab0e2407-2705-f274-e053-dbdaa90a6471	7dea36eb-93bf-4593-9160-c84dfec26ab5

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
63739-165-10	EA - Each	63739-165	764d6e85-9a1e-44b3-85b0-30ff8760a0d9	1	2013-02-13

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63739-165-10	63739016510	10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-165-10) > 10 TABLET in 1 BLISTER PACK	10 blister pack	1988-08-08	2021-07-31	No	No	Current