What is NDC 62756-299?

62756-299 is the product NDC for phenytoin sodium, Phenytoin sodium 200 mg/1 capsule, extended release, listed with the FDA by Sun Pharmaceutical Industries, Inc.. It has 4 package NDCs, shown above in 10- and 11-digit form.

Sun Pharmaceutical Industries, Inc., NDC labeler code 62756. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for phenytoin sodium?

26 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

phenytoin sodium NDC 62756-299 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)62756-299Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62756-0299Add 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 NDC	11-digit (billing)	Package
62756-299-08	6275602990862756029908	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-299-08)Marketed from Jun 30, 2008
62756-299-13	6275602991362756029913	500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-299-13)Marketed from Jun 30, 2008
62756-299-83	6275602998362756029983	30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-299-83)Marketed from Jun 30, 2008
62756-299-88	6275602998862756029988	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-299-88)Marketed from Jun 30, 2008

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): phenytoin sodium
Generic name (nonproprietary): phenytoin sodium
Active ingredients: Phenytoin sodium — 200 mg/1
Dosage form: Capsule, Extended release
Route: Oral
Labeler: Sun Pharmaceutical Industries, Inc.NDC labeler code 62756
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 040731
Marketing start: Jun 30, 2008
Listing expires: Dec 31, 2026
Other FDA classes: Cytochrome P450 1A2 Inducers (Mechanism)Cytochrome P450 2B6 Inducers (Mechanism)Cytochrome P450 2C19 Inducers (Mechanism)Cytochrome P450 2C8 Inducers (Mechanism)Cytochrome P450 2C9 Inducers (Mechanism)Cytochrome P450 2D6 Inducers (Mechanism)Cytochrome P450 3A Inducers (Mechanism)Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers: Product ID 62756-299_c89dfc75-606c-4a4e-9d2b-d907b492a837SPL ID c89dfc75-606c-4a4e-9d2b-d907b492a837SPL set ID c40f66cc-6f4a-4b29-84ba-d265e4848735RxCUI 855861, 855873UNII 4182431BJHUPC 0362756432833
Pharmacologic class: Anti-epileptic Agent

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

N462756029908 followed by a unit qualifier and the quantity

Package 62756-0299-08. 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 Dec 14, 2022.

Indications (excerpt from the label)

Extended phenytoin sodium capsules are indicated for the treatment of tonic-clonic (grand mal) and psychomotor (temporal lobe) seizures and prevention and treatment of seizures occurring during or following neurosurgery. Extended phenytoin sodium capsules are indicated for the treatment of tonic-clonic (grand mal) and psychomotor (temporal lobe) seizures and prevention and treatment of seizures occurring during or following neurosurgery. (1)

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 62756-299

What is NDC 62756-299?: 62756-299 is the product NDC for phenytoin sodium, Phenytoin sodium 200 mg/1 capsule, extended release, listed with the FDA by Sun Pharmaceutical Industries, Inc.. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: phenytoin sodium.
What is the active ingredient?: Phenytoin sodium.
Who is the labeler?: Sun Pharmaceutical Industries, Inc., NDC labeler code 62756. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for phenytoin sodium?: 26 other product NDCs are listed under this name. See all phenytoin sodium NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other phenytoin sodium NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Phenytoin Sodium	Phenytoin sodium 100 mg/1	Capsule, Extended releaseOral	Coupler LLC	67046-0585	67046-0585-03
Phenytoin Sodium	Phenytoin sodium 100 mg/1	Capsule, Extended releaseOral	AvPAK	50268-719	50268-0719-13
Phenytoin Sodium	Phenytoin sodium 100 mg/1	Capsule, Extended releaseOral	Major Pharmaceuticals	0904-7416	00904-7416-61
Phenytoin Sodium	Phenytoin sodium 50 mg/mL	InjectionIntramuscular, Intravenous	Henry Schein, Inc.	0404-9808	00404-9808-05
Phenytoin Sodium	Phenytoin sodium 100 mg/1	Capsule, Extended releaseOral	Unichem Pharmaceuticals (USA), Inc.	29300-379	29300-0379-0129300-0379-0529300-0379-10
Phenytoin Sodium	Phenytoin sodium 50 mg/mL	InjectionIntramuscular, Intravenous	Henry Schein, Inc.	0404-9932	00404-9932-02
Phenytoin Sodium	Phenytoin sodium 50 mg/mL	InjectionIntramuscular, Intravenous	Acella Pharmaceuticals, LLC	42192-614	42192-0614-1042192-0614-30
Phenytoin Sodium	Phenytoin sodium 100 mg/1	Capsule, Extended releaseOral	REMEDYREPACK INC.	70518-2293	70518-2293-0070518-2293-01
Phenytoin Sodium	Phenytoin sodium 50 mg/mL	InjectionIntramuscular, Intravenous	HF Acquisition Co LLC, DBA HealthFirst	51662-1250	51662-1250-01
Phenytoin Sodium	Phenytoin sodium 50 mg/mL	InjectionIntramuscular, Intravenous	HF Acquisition Co LLC, DBA HealthFirst	51662-1251	51662-1251-0151662-1251-03

All 27 phenytoin sodium NDCs

Other NDCs under ANDA 040731

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

FDA NDC Directory listings under ANDA 040731
Product	Strength	Form · route	Labeler	Product NDC
phenytoin sodium	Phenytoin sodium 300 mg/1	Capsule, Extended releaseOral	Sun Pharmaceutical Industries, Inc.	62756-432