Venlafaxine Hydrochloride

Product NDC: 47335-758
11-digit product format: 473350758
Labeler code: 47335
Product ID: 47335-758_dae15132-d26b-4ea9-b937-da9c282ada48
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Venlafaxine Hydrochloride
Dosage form: TABLET, EXTENDED RELEASE
Route: ORAL
Labeler: Sun Pharmaceutical Industries, Inc.
Application: ANDA091272
Marketing category: ANDA
Marketing start: 2014-12-15
Substance: VENLAFAXINE HYDROCHLORIDE
Active strength: 150 mg/1
Pharmacologic classes: Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Source provenance: Browse the complete Orange Book source catalog · source snapshot 44.

Orange Book products#

Current product rows page 1 of 1 · 4 matching rows.

Application-product, Trade name, Ingredient table
Application-product	Trade name	Ingredient	Strength	Dosage form / route	Approval date
A091272-001	VENLAFAXINE HYDROCHLORIDE	VENLAFAXINE HYDROCHLORIDE	EQ 37.5MG BASE	TABLET, EXTENDED RELEASE / ORAL	2010-08-18
A091272-002	VENLAFAXINE HYDROCHLORIDE	VENLAFAXINE HYDROCHLORIDE	EQ 75MG BASE	TABLET, EXTENDED RELEASE / ORAL	2010-08-18
A091272-003	VENLAFAXINE HYDROCHLORIDE	VENLAFAXINE HYDROCHLORIDE	EQ 150MG BASE	TABLET, EXTENDED RELEASE / ORAL	2010-08-18
A091272-004	VENLAFAXINE HYDROCHLORIDE	VENLAFAXINE HYDROCHLORIDE	EQ 225MG BASE	TABLET, EXTENDED RELEASE / ORAL	2019-01-08

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 5 · 176 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	Trade name	Strength	Dosage form / route	Approval date	Source SHA-256
2026-10-15 13:18:30	2026-09	A091272-001	VENLAFAXINE HYDROCHLORIDE	EQ 37.5MG BASE	TABLET, EXTENDED RELEASE / ORAL	2010-08-18	`c2088c7a36db…`
2026-10-15 13:18:30	2026-09	A091272-002	VENLAFAXINE HYDROCHLORIDE	EQ 75MG BASE	TABLET, EXTENDED RELEASE / ORAL	2010-08-18	`c2088c7a36db…`
2026-10-15 13:18:30	2026-09	A091272-003	VENLAFAXINE HYDROCHLORIDE	EQ 150MG BASE	TABLET, EXTENDED RELEASE / ORAL	2010-08-18	`c2088c7a36db…`
2026-10-15 13:18:30	2026-09	A091272-004	VENLAFAXINE HYDROCHLORIDE	EQ 225MG BASE	TABLET, EXTENDED RELEASE / ORAL	2019-01-08	`c2088c7a36db…`
2026-09-14 22:38:34	2026-08	A091272-001	VENLAFAXINE HYDROCHLORIDE	EQ 37.5MG BASE	TABLET, EXTENDED RELEASE / ORAL	2010-08-18	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	A091272-002	VENLAFAXINE HYDROCHLORIDE	EQ 75MG BASE	TABLET, EXTENDED RELEASE / ORAL	2010-08-18	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	A091272-003	VENLAFAXINE HYDROCHLORIDE	EQ 150MG BASE	TABLET, EXTENDED RELEASE / ORAL	2010-08-18	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	A091272-004	VENLAFAXINE HYDROCHLORIDE	EQ 225MG BASE	TABLET, EXTENDED RELEASE / ORAL	2019-01-08	`84e616aacf4f…`
2026-08-18 06:07:40	2026-07	A091272-001	VENLAFAXINE HYDROCHLORIDE	EQ 37.5MG BASE	TABLET, EXTENDED RELEASE / ORAL	2010-08-18	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	A091272-002	VENLAFAXINE HYDROCHLORIDE	EQ 75MG BASE	TABLET, EXTENDED RELEASE / ORAL	2010-08-18	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	A091272-003	VENLAFAXINE HYDROCHLORIDE	EQ 150MG BASE	TABLET, EXTENDED RELEASE / ORAL	2010-08-18	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	A091272-004	VENLAFAXINE HYDROCHLORIDE	EQ 225MG BASE	TABLET, EXTENDED RELEASE / ORAL	2019-01-08	`caaa826d4ba7…`
2026-02-19 14:30 UTC	2026-02	A091272-001	VENLAFAXINE HYDROCHLORIDE	EQ 37.5MG BASE	TABLET, EXTENDED RELEASE / ORAL	2010-08-18	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	A091272-002	VENLAFAXINE HYDROCHLORIDE	EQ 75MG BASE	TABLET, EXTENDED RELEASE / ORAL	2010-08-18	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	A091272-003	VENLAFAXINE HYDROCHLORIDE	EQ 150MG BASE	TABLET, EXTENDED RELEASE / ORAL	2010-08-18	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	A091272-004	VENLAFAXINE HYDROCHLORIDE	EQ 225MG BASE	TABLET, EXTENDED RELEASE / ORAL	2019-01-08	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A091272-001	VENLAFAXINE HYDROCHLORIDE	EQ 37.5MG BASE	TABLET, EXTENDED RELEASE / ORAL	2010-08-18	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A091272-002	VENLAFAXINE HYDROCHLORIDE	EQ 75MG BASE	TABLET, EXTENDED RELEASE / ORAL	2010-08-18	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A091272-003	VENLAFAXINE HYDROCHLORIDE	EQ 150MG BASE	TABLET, EXTENDED RELEASE / ORAL	2010-08-18	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A091272-004	VENLAFAXINE HYDROCHLORIDE	EQ 225MG BASE	TABLET, EXTENDED RELEASE / ORAL	2019-01-08	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	A091272-001	VENLAFAXINE HYDROCHLORIDE	EQ 37.5MG BASE	TABLET, EXTENDED RELEASE / ORAL	2010-08-18	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	A091272-002	VENLAFAXINE HYDROCHLORIDE	EQ 75MG BASE	TABLET, EXTENDED RELEASE / ORAL	2010-08-18	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	A091272-003	VENLAFAXINE HYDROCHLORIDE	EQ 150MG BASE	TABLET, EXTENDED RELEASE / ORAL	2010-08-18	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	A091272-004	VENLAFAXINE HYDROCHLORIDE	EQ 225MG BASE	TABLET, EXTENDED RELEASE / ORAL	2019-01-08	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A091272-001	VENLAFAXINE HYDROCHLORIDE	EQ 37.5MG BASE	TABLET, EXTENDED RELEASE / ORAL	2010-08-18	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A091272-002	VENLAFAXINE HYDROCHLORIDE	EQ 75MG BASE	TABLET, EXTENDED RELEASE / ORAL	2010-08-18	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A091272-003	VENLAFAXINE HYDROCHLORIDE	EQ 150MG BASE	TABLET, EXTENDED RELEASE / ORAL	2010-08-18	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A091272-004	VENLAFAXINE HYDROCHLORIDE	EQ 225MG BASE	TABLET, EXTENDED RELEASE / ORAL	2019-01-08	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A091272-001	VENLAFAXINE HYDROCHLORIDE	EQ 37.5MG BASE	TABLET, EXTENDED RELEASE / ORAL	2010-08-18	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A091272-002	VENLAFAXINE HYDROCHLORIDE	EQ 75MG BASE	TABLET, EXTENDED RELEASE / ORAL	2010-08-18	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A091272-003	VENLAFAXINE HYDROCHLORIDE	EQ 150MG BASE	TABLET, EXTENDED RELEASE / ORAL	2010-08-18	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A091272-004	VENLAFAXINE HYDROCHLORIDE	EQ 225MG BASE	TABLET, EXTENDED RELEASE / ORAL	2019-01-08	`b8a1b40f171c…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A091272-001	VENLAFAXINE HYDROCHLORIDE	EQ 37.5MG BASE	TABLET, EXTENDED RELEASE / ORAL	2010-08-18	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A091272-002	VENLAFAXINE HYDROCHLORIDE	EQ 75MG BASE	TABLET, EXTENDED RELEASE / ORAL	2010-08-18	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A091272-003	VENLAFAXINE HYDROCHLORIDE	EQ 150MG BASE	TABLET, EXTENDED RELEASE / ORAL	2010-08-18	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A091272-004	VENLAFAXINE HYDROCHLORIDE	EQ 225MG BASE	TABLET, EXTENDED RELEASE / ORAL	2019-01-08	`03ed91905a0d…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A091272-001	VENLAFAXINE HYDROCHLORIDE	EQ 37.5MG BASE	TABLET, EXTENDED RELEASE / ORAL	2010-08-18	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A091272-002	VENLAFAXINE HYDROCHLORIDE	EQ 75MG BASE	TABLET, EXTENDED RELEASE / ORAL	2010-08-18	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A091272-003	VENLAFAXINE HYDROCHLORIDE	EQ 150MG BASE	TABLET, EXTENDED RELEASE / ORAL	2010-08-18	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A091272-004	VENLAFAXINE HYDROCHLORIDE	EQ 225MG BASE	TABLET, EXTENDED RELEASE / ORAL	2019-01-08	`2680178bc6a6…`

Observed Orange Book normalized TE history#

Normalized TE history page 2 of 4 · 132 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	TE code	Order	Source SHA-256
2019-12-13 00:20 UTC	2019-12	A091272-001	AB	1	`74a2ff9319b5…`
2019-12-13 00:20 UTC	2019-12	A091272-002	AB	1	`74a2ff9319b5…`
2019-12-13 00:20 UTC	2019-12	A091272-003	AB	1	`74a2ff9319b5…`
2019-12-13 00:20 UTC	2019-12	A091272-004	AB	1	`74a2ff9319b5…`
2022-03-09 01:35 UTC	2022-03	A091272-001	AB	1	`bb7c543d1eb4…`
2022-03-09 01:35 UTC	2022-03	A091272-002	AB	1	`bb7c543d1eb4…`
2022-03-09 01:35 UTC	2022-03	A091272-003	AB	1	`bb7c543d1eb4…`
2022-03-09 01:35 UTC	2022-03	A091272-004	AB	1	`bb7c543d1eb4…`
2021-12-28 21:50 UTC	2021-12	A091272-001	AB	1	`782e0a99824c…`
2021-12-28 21:50 UTC	2021-12	A091272-002	AB	1	`782e0a99824c…`
2021-12-28 21:50 UTC	2021-12	A091272-003	AB	1	`782e0a99824c…`
2021-12-28 21:50 UTC	2021-12	A091272-004	AB	1	`782e0a99824c…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	A091272-001	AB	1	`87673890dc5c…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	A091272-002	AB	1	`87673890dc5c…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	A091272-003	AB	1	`87673890dc5c…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	A091272-004	AB	1	`87673890dc5c…`
2021-03-12 10:30 UTC	2021-03	A091272-001	AB	1	`5aa47cf7b7d7…`
2021-03-12 10:30 UTC	2021-03	A091272-002	AB	1	`5aa47cf7b7d7…`
2021-03-12 10:30 UTC	2021-03	A091272-003	AB	1	`5aa47cf7b7d7…`
2021-03-12 10:30 UTC	2021-03	A091272-004	AB	1	`5aa47cf7b7d7…`
2020-12-22 03:56 UTC	2020-12	A091272-001	AB	1	`8869cabd3fbd…`
2020-12-22 03:56 UTC	2020-12	A091272-002	AB	1	`8869cabd3fbd…`
2020-12-22 03:56 UTC	2020-12	A091272-003	AB	1	`8869cabd3fbd…`
2020-12-22 03:56 UTC	2020-12	A091272-004	AB	1	`8869cabd3fbd…`
2020-11-12 02:37 UTC	2020-11	A091272-001	AB	1	`c0c555d07b60…`
2020-11-12 02:37 UTC	2020-11	A091272-002	AB	1	`c0c555d07b60…`
2020-11-12 02:37 UTC	2020-11	A091272-003	AB	1	`c0c555d07b60…`
2020-11-12 02:37 UTC	2020-11	A091272-004	AB	1	`c0c555d07b60…`
2019-12-14 00:12 UTC	2019-12	A091272-001	AB	1	`3f01610625f2…`
2019-12-14 00:12 UTC	2019-12	A091272-002	AB	1	`3f01610625f2…`
2019-12-14 00:12 UTC	2019-12	A091272-003	AB	1	`3f01610625f2…`
2019-12-14 00:12 UTC	2019-12	A091272-004	AB	1	`3f01610625f2…`
2019-09-15 20:21 UTC	2019-09	A091272-001	AB	1	`b00525d2431f…`
2019-09-15 20:21 UTC	2019-09	A091272-002	AB	1	`b00525d2431f…`
2019-09-15 20:21 UTC	2019-09	A091272-003	AB	1	`b00525d2431f…`
2019-09-15 20:21 UTC	2019-09	A091272-004	AB	1	`b00525d2431f…`
2019-07-19 19:46 UTC	2019-07	A091272-001	AB	1	`ea99ee380514…`
2019-07-19 19:46 UTC	2019-07	A091272-002	AB	1	`ea99ee380514…`
2019-07-19 19:46 UTC	2019-07	A091272-003	AB	1	`ea99ee380514…`
2019-07-19 19:46 UTC	2019-07	A091272-004	AB	1	`ea99ee380514…`

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: Venlafaxine Hydrochloride
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
VENLAFAXINE HYDROCHLORIDE	150 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
7D7RX5A8MO	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 4 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
808744	Internal RxNorm lookup
808748	Internal RxNorm lookup
808751	Internal RxNorm lookup
808753	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
dc989aa7-c4ab-4359-a971-523eb477ef9b	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
17db3736-056c-48b9-b0f4-00fccabb14e6	Product name	5	20251118
7be8b949-f2c0-bdd8-e89d-8af92c1b2ead	Product name	9	20250224
362d7abb-94e6-4c60-9a58-266894157713	Product name	1	20231023
b1435b59-059c-404b-a587-53656bf80e17	Product name	1	20230314
816b97af-edc5-4060-aff1-b814bdbcad50	Product name	1	20190415
6005cd75-f7b1-d6be-3cb5-4bd30d5c4617	Product name	3	20190314
419aab54-5d5a-4146-9453-026d4a9991be	Product name	2	20170525
89dac932-b90a-4410-9ab1-84c53e57de25	Product name	1	20150316
d723478e-ad4a-ec23-6bd7-cfe33e1e3840	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
47335-758-08	Venlafaxine Hydrochloride	100 in 1 BOTTLE	TABLET, EXTENDED RELEASE	100	12
47335-758-18	Venlafaxine Hydrochloride	1000 in 1 BOTTLE	TABLET, EXTENDED RELEASE	1000	12
47335-758-81	Venlafaxine Hydrochloride	90 in 1 BOTTLE	TABLET, EXTENDED RELEASE	90	12
47335-758-83	Venlafaxine Hydrochloride	30 in 1 BOTTLE	TABLET, EXTENDED RELEASE	30	12
47335-758-88	Venlafaxine Hydrochloride	100 in 1 BOTTLE	TABLET, EXTENDED RELEASE	100	12
47335-758-99	Venlafaxine Hydrochloride	10 in 1 BLISTER PACK	TABLET, EXTENDED RELEASE	10	12
47335-758-99	Venlafaxine Hydrochloride	2 in 1 BOX, UNIT-DOSE	TABLET, EXTENDED RELEASE	2	12

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
47335-758-81	EA - Each	47335-758	3b2f25aa-1fc1-4f65-827d-689d138e1434	1	2018-05-09
47335-758-83	EA - Each	47335-758	9d4b8672-cae4-495a-ac06-bcf8cf64f390	1	2018-05-09

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
VENLAFAXINE HYDROCHLORIDE	ACTIVE INGREDIENT	7D7RX5A8MO	VENLAFAXINE HYDROCHLORIDE TABLET, EXTENDED RELEASE [SUN PHARMA GLOBAL FZE]	1
VENLAFAXINE	ACTIVE MOIETY	GRZ5RCB1QG	VENLAFAXINE HYDROCHLORIDE TABLET, EXTENDED RELEASE [SUN PHARMA GLOBAL FZE]	1
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	VENLAFAXINE HYDROCHLORIDE TABLET, EXTENDED RELEASE [SUN PHARMA GLOBAL FZE]	1
CROSPOVIDONE	INACTIVE INGREDIENT	68401960MK	VENLAFAXINE HYDROCHLORIDE TABLET, EXTENDED RELEASE [SUN PHARMA GLOBAL FZE]	1
DIBUTYL SEBACATE	INACTIVE INGREDIENT	4W5IH7FLNY	VENLAFAXINE HYDROCHLORIDE TABLET, EXTENDED RELEASE [SUN PHARMA GLOBAL FZE]	1
FD&C RED NO. 40	INACTIVE INGREDIENT	WZB9127XOA	VENLAFAXINE HYDROCHLORIDE TABLET, EXTENDED RELEASE [SUN PHARMA GLOBAL FZE]	1
HYPROMELLOSE 2208 (4000 MPA.S)	INACTIVE INGREDIENT	39J80LT57T	VENLAFAXINE HYDROCHLORIDE TABLET, EXTENDED RELEASE [SUN PHARMA GLOBAL FZE]	1
LACTOSE MONOHYDRATE	INACTIVE INGREDIENT	EWQ57Q8I5X	VENLAFAXINE HYDROCHLORIDE TABLET, EXTENDED RELEASE [SUN PHARMA GLOBAL FZE]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	VENLAFAXINE HYDROCHLORIDE TABLET, EXTENDED RELEASE [SUN PHARMA GLOBAL FZE]	1
MANNITOL	INACTIVE INGREDIENT	3OWL53L36A	VENLAFAXINE HYDROCHLORIDE TABLET, EXTENDED RELEASE [SUN PHARMA GLOBAL FZE]	1
METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A	INACTIVE INGREDIENT	NX76LV5T8J	VENLAFAXINE HYDROCHLORIDE TABLET, EXTENDED RELEASE [SUN PHARMA GLOBAL FZE]	1
POLYETHYLENE GLYCOL 3350	INACTIVE INGREDIENT	G2M7P15E5P	VENLAFAXINE HYDROCHLORIDE TABLET, EXTENDED RELEASE [SUN PHARMA GLOBAL FZE]	1
POLYSORBATE 20	INACTIVE INGREDIENT	7T1F30V5YH	VENLAFAXINE HYDROCHLORIDE TABLET, EXTENDED RELEASE [SUN PHARMA GLOBAL FZE]	1
POLYSORBATE 80	INACTIVE INGREDIENT	6OZP39ZG8H	VENLAFAXINE HYDROCHLORIDE TABLET, EXTENDED RELEASE [SUN PHARMA GLOBAL FZE]	1
POLYVINYL ALCOHOL	INACTIVE INGREDIENT	532B59J990	VENLAFAXINE HYDROCHLORIDE TABLET, EXTENDED RELEASE [SUN PHARMA GLOBAL FZE]	1
POVIDONE K30	INACTIVE INGREDIENT	U725QWY32X	VENLAFAXINE HYDROCHLORIDE TABLET, EXTENDED RELEASE [SUN PHARMA GLOBAL FZE]	1
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	VENLAFAXINE HYDROCHLORIDE TABLET, EXTENDED RELEASE [SUN PHARMA GLOBAL FZE]	1
SODIUM LAURYL SULFATE	INACTIVE INGREDIENT	368GB5141J	VENLAFAXINE HYDROCHLORIDE TABLET, EXTENDED RELEASE [SUN PHARMA GLOBAL FZE]	1
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	VENLAFAXINE HYDROCHLORIDE TABLET, EXTENDED RELEASE [SUN PHARMA GLOBAL FZE]	1
TRIETHYL CITRATE	INACTIVE INGREDIENT	8Z96QXD6UM	VENLAFAXINE HYDROCHLORIDE TABLET, EXTENDED RELEASE [SUN PHARMA GLOBAL FZE]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
47335-758	VENLAFAXINE HYDROCHLORIDE TABLET, EXTENDED RELEASE [SUN PHARMACEUTICAL INDUSTRIES, INC.]	12	Current NDC, Legacy NDC, 7 package rows	20230916_dc989aa7-c4ab-4359-a971-523eb477ef9b.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
Venlafaxine Hydrochloride	VENLAFAXINE HYDROCHLORIDE	Sun Pharmaceutical Industries, Inc.	dc989aa7-c4ab-4359-a971-523eb477ef9b	2023-09-15	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 091272 application number: ANDA091272 ndc (product): 47335-758

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
7D7RX5A8MO	VENLAFAXINE HYDROCHLORIDE	99300-78-4	VENLAFAXINE HYDROCHLORIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
808744	venlafaxine HCl 150 MG 24HR Extended Release Oral Tablet	PSN	dc989aa7-c4ab-4359-a971-523eb477ef9b	12
808748	venlafaxine HCl 225 MG 24HR Extended Release Oral Tablet	PSN	dc989aa7-c4ab-4359-a971-523eb477ef9b	12
808751	venlafaxine HCl 37.5 MG 24HR Extended Release Oral Tablet	PSN	dc989aa7-c4ab-4359-a971-523eb477ef9b	12
808753	venlafaxine HCl 75 MG 24HR Extended Release Oral Tablet	PSN	dc989aa7-c4ab-4359-a971-523eb477ef9b	12
808744	24 HR venlafaxine 150 MG Extended Release Oral Tablet	SCD	dc989aa7-c4ab-4359-a971-523eb477ef9b	12
808748	24 HR venlafaxine 225 MG Extended Release Oral Tablet	SCD	dc989aa7-c4ab-4359-a971-523eb477ef9b	12
808751	24 HR venlafaxine 37.5 MG Extended Release Oral Tablet	SCD	dc989aa7-c4ab-4359-a971-523eb477ef9b	12
808753	24 HR venlafaxine 75 MG Extended Release Oral Tablet	SCD	dc989aa7-c4ab-4359-a971-523eb477ef9b	12
808744	venlafaxine 150 MG (as venlafaxine hydrochloride) 24 HR Extended Release Oral Tablet	SY	dc989aa7-c4ab-4359-a971-523eb477ef9b	12
808744	venlafaxine 150 MG 24 HR Extended Release Oral Tablet	SY	dc989aa7-c4ab-4359-a971-523eb477ef9b	12
808748	venlafaxine 225 MG (as venlafaxine hydrochloride) 24 HR Extended Release Oral Tablet	SY	dc989aa7-c4ab-4359-a971-523eb477ef9b	12
808748	venlafaxine 225 MG 24 HR Extended Release Oral Tablet	SY	dc989aa7-c4ab-4359-a971-523eb477ef9b	12
808751	venlafaxine 37.5 MG (as venlafaxine hydrochloride) 24 HR Extended Release Oral Tablet	SY	dc989aa7-c4ab-4359-a971-523eb477ef9b	12
808751	venlafaxine 37.5 MG 24 HR Extended Release Oral Tablet	SY	dc989aa7-c4ab-4359-a971-523eb477ef9b	12
808753	venlafaxine 75 MG (as venlafaxine hydrochloride) 24 HR Extended Release Oral Tablet	SY	dc989aa7-c4ab-4359-a971-523eb477ef9b	12
808753	venlafaxine 75 MG 24 HR Extended Release Oral Tablet	SY	dc989aa7-c4ab-4359-a971-523eb477ef9b	12

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
47335-758-08	47335075808	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-758-08)		2014-12-15	0000-00-00	No	No	Current
47335-758-18	47335075818	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-758-18)		2014-12-15	0000-00-00	No	No	Current
47335-758-81	47335075881	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-758-81)		2014-12-15	0000-00-00	No	No	Current
47335-758-83	47335075883	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-758-83)		2014-12-15	0000-00-00	No	No	Current
47335-758-88	47335075888	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-758-88)		2014-12-15	0000-00-00	No	No	Current
47335-758-99	47335075899	2 BLISTER PACK in 1 BOX, UNIT-DOSE (47335-758-99) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK	2 blister pack	2019-03-29	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Venlafaxine Hydrochloride	Sun Pharmaceutical Industries, Inc. \| Sun Pharmaceutical Industries Limited	2023-09-15	Human Prescription Drug Label	12
Venlafaxine Hydrochloride	REMEDYREPACK INC.	2022-04-20	HUMAN PRESCRIPTION DRUG LABEL	3