Prescription drug · ANDA

Venlafaxine Hydrochloride NDC 70710-1700

Venlafaxine hydrochloride 150 mg/1 · Capsule, Extended release · Oral · Zydus Pharmaceuticals USA Inc.

NDC codes

FDA NDC Directory
Product NDC (as listed)70710-1700Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70710-1700Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
70710-1700-0707101700001000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70710-1700-0)Marketed from May 18, 2023
70710-1700-37071017000330 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70710-1700-3)Marketed from May 18, 2023
70710-1700-47071017000410 BLISTER PACK in 1 CARTON (70710-1700-4) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70710-1700-2)Marketed from May 18, 2023
70710-1700-570710170005500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70710-1700-5)Marketed from May 18, 2023
70710-1700-97071017000990 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70710-1700-9)Marketed from May 18, 2023

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Venlafaxine Hydrochloride
Generic name (nonproprietary)
venlafaxine hydrochloride
Active ingredients
Venlafaxine hydrochloride — 150 mg/1
Dosage form
Capsule, Extended release
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 090174
Marketing start
Listing expires
Other FDA classes
Norepinephrine Uptake Inhibitors (Mechanism)Serotonin Uptake Inhibitors (Mechanism)
Identifiers
Product ID 70710-1700_9d291423-f1d9-4605-af7c-f18537aa8914SPL ID 9d291423-f1d9-4605-af7c-f18537aa8914SPL set ID 9fda0f8d-b24e-4581-9dca-7aaaf86e2413RxCUI 313581, 313583, 313585UNII 7D7RX5A8MOUPC 0370710170097, 0370710169992

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N470710170000 followed by a unit qualifier and the quantity

Package 70710-1700-00. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective . This label includes a boxed warning.

Indications (excerpt from the label)

Venlafaxine hydrochloride extended-release capsules are indicated in adults for the treatment of: Major Depressive Disorder (MDD) [see Clinical Studies ( 14.1 )] Generalized Anxiety Disorder (GAD) [see Clinical Studies ( 14.2 )] Social Anxiety Disorder (SAD) [see Clinical Studies ( 14.3 )] Panic Disorder (PD) [see Clinical Studies ( 14.4 )] Venlafaxine hydrochloride extended-release capsules are a serotonin and norepinephrine reuptake inhibitor (SNRI) indicated for the treatment of adults with: Major Depressive Disorder (MDD) ( 1 ) Generalized Anxiety Disorder (GAD) ( 1 ) Social Anxiety Disorder (SAD) ( 1 ) Panic Disorder (PD) ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 090174

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 090174
ProductStrengthForm · routeLabelerProduct NDC
Venlafaxine HydrochlorideVenlafaxine hydrochloride 150 mg/1Capsule, Extended releaseOralPreferred Pharmaceuticals Inc.68788-8774
venlafaxine hydrochlorideVenlafaxine hydrochloride 150 mg/1Capsule, Extended releaseOralPreferred Pharmaceuticals Inc.68788-6806
venlafaxine hydrochlorideVenlafaxine hydrochloride 150 mg/1Capsule, Extended releaseOralNuCare Pharmaceuticals,Inc.68071-4442
venlafaxine hydrochlorideVenlafaxine hydrochloride 75 mg/1Capsule, Extended releaseOralZydus Lifesciences Limited65841-752
venlafaxine hydrochlorideVenlafaxine hydrochloride 37.5 mg/1Capsule, Extended releaseOralZydus Lifesciences Limited65841-751
venlafaxine hydrochlorideVenlafaxine hydrochloride 150 mg/1Capsule, Extended releaseOralZydus Lifesciences Limited65841-753
venlafaxine hydrochlorideVenlafaxine hydrochloride 37.5 mg/1Capsule, Extended releaseOralZydus Pharmaceuticals USA Inc.68382-034
venlafaxine hydrochlorideVenlafaxine hydrochloride 75 mg/1Capsule, Extended releaseOralZydus Pharmaceuticals USA Inc.68382-035
venlafaxine hydrochlorideVenlafaxine hydrochloride 150 mg/1Capsule, Extended releaseOralZydus Pharmaceuticals USA Inc.68382-036
Venlafaxine HydrochlorideVenlafaxine hydrochloride 150 mg/1Capsule, Extended releaseOralZydus Lifesciences Limited70771-1838
Venlafaxine HydrochlorideVenlafaxine hydrochloride 37.5 mg/1Capsule, Extended releaseOralZydus Lifesciences Limited70771-1836
Venlafaxine HydrochlorideVenlafaxine hydrochloride 75 mg/1Capsule, Extended releaseOralZydus Lifesciences Limited70771-1837
Venlafaxine HydrochlorideVenlafaxine hydrochloride 75 mg/1Capsule, Extended releaseOralZydus Pharmaceuticals USA Inc.70710-1699
Venlafaxine HydrochlorideVenlafaxine hydrochloride 37.5 mg/1Capsule, Extended releaseOralZydus Pharmaceuticals USA Inc.70710-1698
venlafaxine hydrochlorideVenlafaxine hydrochloride 37.5 mg/1Capsule, Extended releaseOralA-S Medication Solutions50090-6301
venlafaxine hydrochlorideVenlafaxine hydrochloride 75 mg/1Capsule, Extended releaseOralBryant Ranch Prepack71335-1338

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