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HEPARIN SODIUM INJECTION 10,000U/ML 25X1ML VIAL

Generic: Heparin Sodium

NDC:63739-0964-25

Manufacturer:McKesson Corporation dba SKY Packaging

Strength:10000 [USP'U]/mL

Dosage Form:INJECTION, SOLUTION

Route:INTRAVENOUS, SUBCUTANEOUS

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Drug Information

Identification

Generic Name

Heparin Sodium

Brand Name

Heparin Sodium

Labeler / Distributor

McKesson Corporation dba SKY Packaging

Product Type

HUMAN PRESCRIPTION DRUG

Administration

Dosage Form

INJECTION, SOLUTION

Route of Administration

INTRAVENOUS, SUBCUTANEOUS

FDA Application Number

ANDA203198

Active Ingredients

Ingredient	Strength
HEPARIN SODIUM	10000 [USP'U]/mL

Pharmacological Class

Anti-coagulantHeparin [CS]Unfractionated Heparin

Data sourced from openFDA / DailyMed. For full prescribing information, consult the drug label.

Wholesale compliance resources

DSCSA T2 documents DSCSA compliance resource hub

Drug Resources

Heparin sodium Drug Page NDC 63739-0964-25 Lookup

Clinical Drug Information

Indications & Usage

Use for relief of occasional sleeplessness caused by stress and repetitive thoughts

Warnings

Warnings When using this product keep away from eyes Stop use and ask a doctor if sleeplessness persists for more than two weeks: insomnia can be a symptom of serious underlying medical illness If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Dosage & Administration

Directions adults: apply 2 sprays onto the tongue. Additional sprays may be taken during the night as needed. children under 12: ask a doctor

Clinical data sourced from openFDA drug labeling. For complete prescribing information, consult the full drug label.