Diltiazem Hydrochloride

Product NDC: 63739-079
11-digit product format: 637390079
Labeler code: 63739
Product ID: 63739-079_b3c8103c-9f53-25da-e053-2a95a90a62f9
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Diltiazem Hydrochloride
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: McKesson Corporation dba SKY Packaging
Application: ANDA074185
Marketing category: ANDA
Marketing start: 1995-12-22
Marketing end: 2021-04-30
Substance: DILTIAZEM HYDROCHLORIDE
Active strength: 30 mg/1
Pharmacologic classes: Calcium Channel Antagonists [MoA],Calcium Channel Blocker [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
63739-079-10	2020-07-22	C162847	48780-1	ab0e2407-2735-f274-e053-dbdaa90a6471	da1c1a8e-c9dd-4c20-b061-638f2d0cecda

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
63739-079-10	EA - Each	63739-079	1d82dde6-87b6-45f9-b13b-ffb1ce421bdd	1	2012-07-24

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
OLH94387TE	DILTIAZEM HYDROCHLORIDE	33286-22-5	DILTIAZEM HYDROCHLORIDE

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63739-079-10	63739007910	10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-079-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK	10 blister pack	1995-12-22	2021-04-30	No	No	Current