Diltiazem Hydrochloride

Product NDC: 70436-197
Requested package NDC: 70436-197-06
11-digit product format: 704360197
Labeler code: 70436
Product ID: 70436-197_58494981-80ca-63f9-e063-6294a90aef59
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Diltiazem Hydrochloride
Dosage form: TABLET, EXTENDED RELEASE
Route: ORAL
Labeler: Slate Run Pharmaceuticals, LLC
Application: ANDA216439
Marketing category: ANDA
Marketing start: 2023-03-20
Substance: DILTIAZEM HYDROCHLORIDE
Active strength: 240 mg/1
Pharmacologic classes: Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A4 Inhibitors [MoA]
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

Source provenance: Browse the complete Orange Book source catalog · source snapshot 43.

Orange Book products#

Current product rows page 1 of 1 · 6 matching rows.

Application-product, Trade name, Ingredient table
Application-product	Trade name	Ingredient	Strength	Dosage form / route	TE codes	Approval date
A216439-001	DILTIAZEM HYDROCHLORIDE	DILTIAZEM HYDROCHLORIDE	120MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07
A216439-002	DILTIAZEM HYDROCHLORIDE	DILTIAZEM HYDROCHLORIDE	180MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07
A216439-003	DILTIAZEM HYDROCHLORIDE	DILTIAZEM HYDROCHLORIDE	240MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07
A216439-004	DILTIAZEM HYDROCHLORIDE	DILTIAZEM HYDROCHLORIDE	300MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07
A216439-005	DILTIAZEM HYDROCHLORIDE	DILTIAZEM HYDROCHLORIDE	360MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07
A216439-006	DILTIAZEM HYDROCHLORIDE	DILTIAZEM HYDROCHLORIDE	420MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07

Therapeutic equivalence codes#

Current TE-code rows page 1 of 1 · 6 matching rows.

Application-product, TE code table
Application-product	TE code
A216439-001	AB
A216439-002	AB
A216439-003	AB
A216439-004	AB
A216439-005	AB
A216439-006	AB

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Product history page 1 of 4 · 150 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	Trade name	Strength	Dosage form / route	Product TE source text	Approval date	Source SHA-256
2026-09-14 22:38:34	2026-08	A216439-001	DILTIAZEM HYDROCHLORIDE	120MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	A216439-002	DILTIAZEM HYDROCHLORIDE	180MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	A216439-003	DILTIAZEM HYDROCHLORIDE	240MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	A216439-004	DILTIAZEM HYDROCHLORIDE	300MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	A216439-005	DILTIAZEM HYDROCHLORIDE	360MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	A216439-006	DILTIAZEM HYDROCHLORIDE	420MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`84e616aacf4f…`
2026-08-18 06:07:40	2026-07	A216439-001	DILTIAZEM HYDROCHLORIDE	120MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	A216439-002	DILTIAZEM HYDROCHLORIDE	180MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	A216439-003	DILTIAZEM HYDROCHLORIDE	240MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	A216439-004	DILTIAZEM HYDROCHLORIDE	300MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	A216439-005	DILTIAZEM HYDROCHLORIDE	360MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	A216439-006	DILTIAZEM HYDROCHLORIDE	420MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`caaa826d4ba7…`
2026-02-19 14:30 UTC	2026-02	A216439-001	DILTIAZEM HYDROCHLORIDE	120MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	A216439-002	DILTIAZEM HYDROCHLORIDE	180MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	A216439-003	DILTIAZEM HYDROCHLORIDE	240MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	A216439-004	DILTIAZEM HYDROCHLORIDE	300MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	A216439-005	DILTIAZEM HYDROCHLORIDE	360MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	A216439-006	DILTIAZEM HYDROCHLORIDE	420MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A216439-001	DILTIAZEM HYDROCHLORIDE	120MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A216439-002	DILTIAZEM HYDROCHLORIDE	180MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A216439-003	DILTIAZEM HYDROCHLORIDE	240MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A216439-004	DILTIAZEM HYDROCHLORIDE	300MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A216439-005	DILTIAZEM HYDROCHLORIDE	360MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A216439-006	DILTIAZEM HYDROCHLORIDE	420MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	A216439-001	DILTIAZEM HYDROCHLORIDE	120MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	A216439-002	DILTIAZEM HYDROCHLORIDE	180MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	A216439-003	DILTIAZEM HYDROCHLORIDE	240MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	A216439-004	DILTIAZEM HYDROCHLORIDE	300MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	A216439-005	DILTIAZEM HYDROCHLORIDE	360MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	A216439-006	DILTIAZEM HYDROCHLORIDE	420MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A216439-001	DILTIAZEM HYDROCHLORIDE	120MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A216439-002	DILTIAZEM HYDROCHLORIDE	180MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A216439-003	DILTIAZEM HYDROCHLORIDE	240MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A216439-004	DILTIAZEM HYDROCHLORIDE	300MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A216439-005	DILTIAZEM HYDROCHLORIDE	360MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A216439-006	DILTIAZEM HYDROCHLORIDE	420MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A216439-001	DILTIAZEM HYDROCHLORIDE	120MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A216439-002	DILTIAZEM HYDROCHLORIDE	180MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A216439-003	DILTIAZEM HYDROCHLORIDE	240MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A216439-004	DILTIAZEM HYDROCHLORIDE	300MG	TABLET, EXTENDED RELEASE / ORAL	AB	2023-03-07	`b8a1b40f171c…`

Observed Orange Book normalized TE history#

Normalized TE history page 1 of 4 · 150 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	TE code	Order	Source SHA-256
2026-09-14 22:38:34	2026-08	A216439-001	AB	1	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	A216439-002	AB	1	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	A216439-003	AB	1	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	A216439-004	AB	1	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	A216439-005	AB	1	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	A216439-006	AB	1	`84e616aacf4f…`
2026-08-18 06:07:40	2026-07	A216439-001	AB	1	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	A216439-002	AB	1	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	A216439-003	AB	1	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	A216439-004	AB	1	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	A216439-005	AB	1	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	A216439-006	AB	1	`caaa826d4ba7…`
2026-02-19 14:30 UTC	2026-02	A216439-001	AB	1	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	A216439-002	AB	1	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	A216439-003	AB	1	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	A216439-004	AB	1	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	A216439-005	AB	1	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	A216439-006	AB	1	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A216439-001	AB	1	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A216439-002	AB	1	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A216439-003	AB	1	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A216439-004	AB	1	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A216439-005	AB	1	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A216439-006	AB	1	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	A216439-001	AB	1	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	A216439-002	AB	1	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	A216439-003	AB	1	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	A216439-004	AB	1	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	A216439-005	AB	1	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	A216439-006	AB	1	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A216439-001	AB	1	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A216439-002	AB	1	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A216439-003	AB	1	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A216439-004	AB	1	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A216439-005	AB	1	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A216439-006	AB	1	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A216439-001	AB	1	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A216439-002	AB	1	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A216439-003	AB	1	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A216439-004	AB	1	`b8a1b40f171c…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product: Yes
Brand name base: Diltiazem Hydrochloride
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
DILTIAZEM HYDROCHLORIDE	240 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
OLH94387TE	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 6 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
830874	Internal RxNorm lookup
830877	Internal RxNorm lookup
830879	Internal RxNorm lookup
830882	Internal RxNorm lookup
830897	Internal RxNorm lookup
830900	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
f7137458-0db3-7ecd-e053-6394a90a5f95	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
61ebbccf-eedf-453b-940e-dba67b7a5fef	Product name	4	20260107
a8d6eaa3-afcc-47e5-be12-0c9251fc8740	Product name	1	20251124
f6700316-a6ba-5e59-3413-8ede05ae58b9	Product name	7	20250625
8615f7a1-1e8f-8281-8601-d7a637926d1f	Product name	4	20250522
3a9daa2f-bcd1-13de-a1b4-6172caa7f308	Product name	2	20240419
f7129636-cba8-86c2-8bfb-9e2e2a9c7628	Product name	2	20240314
378290be-e30f-0e68-1201-165e93c337e8	Product name	3	20231212
c733b56e-b0b5-4495-9857-0256a8242279	Product name	1	20220520
f4df4721-60d9-7fd2-a665-5c3c9f55af81	Product name	2	20171003

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70436-197-04	Diltiazem Hydrochloride	30 in 1 BOTTLE	TABLET, EXTENDED RELEASE	30		9
70436-197-06	Diltiazem Hydrochloride	90 in 1 BOTTLE	TABLET, EXTENDED RELEASE	90		9

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
70436-197-04	EA - Each	70436-197	83d60a8e-8a46-493e-9c2d-1551c4f6d5b3	1	2023-04-07
70436-197-06	EA - Each	70436-197	137509c8-4f9f-415e-9376-3521ae54b53a	1	2023-04-07

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70436-197	DILTIAZEM HYDROCHLORIDE TABLET, EXTENDED RELEASE [SLATE RUN PHARMACEUTICALS, LLC]	6	Current NDC, 2 package rows	20240620_f7137458-0db3-7ecd-e053-6394a90a5f95.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Diltiazem Hydrochloride	DILTIAZEM HYDROCHLORIDE	Slate Run Pharmaceuticals, LLC	f7137458-0db3-7ecd-e053-6394a90a5f95	2026-08-05	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 216439 application number: ANDA216439 ndc (package): 70436-197-06 ndc (product): 70436-197 ndc11 (package): 70436019706

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

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
830874	dilTIAZem hydrochloride 120 MG 24HR Extended Release Oral Tablet	PSN	f7137458-0db3-7ecd-e053-6394a90a5f95	9
830877	dilTIAZem hydrochloride 180 MG 24HR Extended Release Oral Tablet	PSN	f7137458-0db3-7ecd-e053-6394a90a5f95	9
830879	dilTIAZem hydrochloride 240 MG 24HR Extended Release Oral Tablet	PSN	f7137458-0db3-7ecd-e053-6394a90a5f95	9
830882	dilTIAZem hydrochloride 300 MG 24HR Extended Release Oral Tablet	PSN	f7137458-0db3-7ecd-e053-6394a90a5f95	9
830897	dilTIAZem hydrochloride 360 MG 24HR Extended Release Oral Tablet	PSN	f7137458-0db3-7ecd-e053-6394a90a5f95	9
830900	dilTIAZem hydrochloride 420 MG 24HR Extended Release Oral Tablet	PSN	f7137458-0db3-7ecd-e053-6394a90a5f95	9
830874	24 HR diltiazem hydrochloride 120 MG Extended Release Oral Tablet	SCD	f7137458-0db3-7ecd-e053-6394a90a5f95	9
830877	24 HR diltiazem hydrochloride 180 MG Extended Release Oral Tablet	SCD	f7137458-0db3-7ecd-e053-6394a90a5f95	9
830879	24 HR diltiazem hydrochloride 240 MG Extended Release Oral Tablet	SCD	f7137458-0db3-7ecd-e053-6394a90a5f95	9
830882	24 HR diltiazem hydrochloride 300 MG Extended Release Oral Tablet	SCD	f7137458-0db3-7ecd-e053-6394a90a5f95	9
830897	24 HR diltiazem hydrochloride 360 MG Extended Release Oral Tablet	SCD	f7137458-0db3-7ecd-e053-6394a90a5f95	9
830900	24 HR diltiazem hydrochloride 420 MG Extended Release Oral Tablet	SCD	f7137458-0db3-7ecd-e053-6394a90a5f95	9
830874	diltiazem hydrochloride 120 MG 24 HR Extended Release Oral Tablet	SY	f7137458-0db3-7ecd-e053-6394a90a5f95	9
830877	diltiazem hydrochloride 180 MG 24 HR Extended Release Oral Tablet	SY	f7137458-0db3-7ecd-e053-6394a90a5f95	9
830879	diltiazem hydrochloride 240 MG 24 HR Extended Release Oral Tablet	SY	f7137458-0db3-7ecd-e053-6394a90a5f95	9
830882	diltiazem hydrochloride 300 MG 24 HR Extended Release Oral Tablet	SY	f7137458-0db3-7ecd-e053-6394a90a5f95	9
830897	diltiazem hydrochloride 360 MG 24 HR Extended Release Oral Tablet	SY	f7137458-0db3-7ecd-e053-6394a90a5f95	9
830900	diltiazem hydrochloride 420 MG 24 HR Extended Release Oral Tablet	SY	f7137458-0db3-7ecd-e053-6394a90a5f95	9

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Sample	Exclude flag	Status
70436-197-06	70436019706	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-197-06)	2023-03-20	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Diltiazem Hydrochloride	Slate Run Pharmaceuticals, LLC \| Yichang Humanwell Oral Solid Dosage Plant	2026-08-05	HUMAN PRESCRIPTION DRUG LABEL	10