Diltiazem Hydrochloride

Product NDC: 68071-4155
11-digit product format: 680714155
Labeler code: 68071
Product ID: 68071-4155_bb63458f-92d8-3853-e053-2995a90aa3e6
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Diltiazem Hydrochloride
Dosage form: CAPSULE, EXTENDED RELEASE
Route: ORAL
Labeler: NuCare Pharmaceuticals,Inc.
Application: ANDA075116
Marketing category: ANDA
Marketing start: 1999-12-28
Marketing end: 0000-00-00
Substance: DILTIAZEM HYDROCHLORIDE
Active strength: 180 mg/1
Pharmacologic classes: Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]
NDC exclude flag: No
Listing certified through: 2022-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
68071-4155-3	2021-02-15	C162847	48780-1	ba0f9c33-4b8c-a910-e053-dadaa90a0b85	5e0a67db-eb84-4882-e053-2991aa0a5714
68071-4155-3	2021-01-29	C162847	48780-1	ba0f9c33-4b8c-a910-e053-dadaa90a0b85	5e0a67db-eb84-4882-e053-2991aa0a5714

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	Marketing start	Marketing end	Sample	Exclude flag	Status
68071-4155-3	68071415503	300 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68071-4155-3)	2017-11-15	0000-00-00	No	No	Current