NDC 0409-1316

Heparin Sodium

Heparin Sodium

Heparin Sodium is a Intravenous; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Hospira, Inc.. The primary component is Heparin Sodium.

• Product ID: 0409-1316_35c5941d-1c68-4be5-b9c0-a9650ddf12a7
• NDC: 0409-1316
• Product Type: Human Prescription Drug
• Proprietary Name: Heparin Sodium
• Generic Name: Heparin Sodium
• Dosage Form: Injection, Solution
• Route of Administration: INTRAVENOUS; SUBCUTANEOUS
• Marketing Start Date: 2005-03-31
• Marketing Category: ANDA / ANDA
• Application Number: ANDA089522
• Labeler Name: Hospira, Inc.
• Substance Name: HEPARIN SODIUM
• Active Ingredient Strength: 10000 [USP'U]/mL
• Pharm Classes: Anti-coagulant [EPC],Heparin [CS],Unfractionated Heparin [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2022-12-31

Packaging

NDC 0409-1316-32

50 CARTRIDGE in 1 CONTAINER (0409-1316-32) > .5 mL in 1 CARTRIDGE (0409-1316-11)

• Marketing Start Date: 2005-03-31
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0409-1316-13 [00409131613]

Heparin Sodium INJECTION, SOLUTION

• Marketing Category: ANDA
• Application Number: ANDA089522
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2005-03-31
• Marketing End Date: 2009-06-29

NDC 0409-1316-25 [00409131625]

Heparin Sodium INJECTION, SOLUTION

• Marketing Category: ANDA
• Application Number: ANDA089522
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 2007-11-14
• Marketing End Date: 2012-10-01

NDC 0409-1316-12 [00409131612]

Heparin Sodium INJECTION, SOLUTION

• Marketing Category: ANDA
• Application Number: ANDA089522
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2005-03-31
• Marketing End Date: 2009-06-29

NDC 0409-1316-01 [00409131601]

Heparin Sodium INJECTION, SOLUTION

• Marketing Category: ANDA
• Application Number: ANDA089522
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2005-03-31
• Marketing End Date: 2009-06-29

NDC 0409-1316-66 [00409131666]

Heparin Sodium INJECTION, SOLUTION

• Marketing Category: ANDA
• Application Number: ANDA089522
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 2005-02-28
• Marketing End Date: 2010-10-01

NDC 0409-1316-11 [00409131611]

Heparin Sodium INJECTION, SOLUTION

• Marketing Category: ANDA
• Application Number: ANDA089522
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 2005-03-31

NDC 0409-1316-31 [00409131631]

Heparin Sodium INJECTION, SOLUTION

• Marketing Category: ANDA
• Application Number: ANDA089522
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2005-03-31
• Marketing End Date: 2009-06-29

NDC 0409-1316-14 [00409131614]

Heparin Sodium INJECTION, SOLUTION

• Marketing Category: ANDA
• Application Number: ANDA089522
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2005-03-31
• Marketing End Date: 2009-06-29

NDC 0409-1316-02 [00409131602]

Heparin Sodium INJECTION, SOLUTION

• Marketing Category: ANDA
• Application Number: ANDA089522
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2005-03-31
• Marketing End Date: 2009-06-29

NDC 0409-1316-32 [00409131632]

Heparin Sodium INJECTION, SOLUTION

• Marketing Category: ANDA
• Application Number: ANDA089522
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 2005-03-31

Drug Details

Active Ingredients

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

OpenFDA Data

• SPL SET ID: c8c4edd2-ee9e-4558-6b8c-b83adc242a0a
• Manufacturer:
  • Hospira, Inc.
• UNII:
  • ZZ45AB24CA
• RxNorm Concept Unique ID - RxCUI:
  • 1659260
  • 1361853

Pharmacological Class

• Anti-coagulant [EPC]
• Heparin [CS]
• Unfractionated Heparin [EPC]

NDC Crossover Matching brand name "Heparin Sodium" or generic name "Heparin Sodium"

NDC	Brand Name	Generic Name
0069-0043	Heparin Sodium	Heparin Sodium
0069-0058	Heparin Sodium	Heparin Sodium
0069-0059	Heparin Sodium	Heparin Sodium
0069-0062	Heparin Sodium	Heparin Sodium
0069-0137	Heparin Sodium	Heparin Sodium
0264-5705	Heparin Sodium	Heparin Sodium
0409-7651	Heparin Sodium	Heparin Sodium
0409-7620	Heparin Sodium	Heparin Sodium
0409-7650	Heparin Sodium	Heparin Sodium
68083-136	Heparin Sodium	Heparin Sodium
76045-108	Heparin Sodium	Heparin Sodium
0641-0410	Heparin Sodium	Heparin Sodium
0641-0391	Heparin Sodium	Heparin Sodium
0641-0400	Heparin Sodium	Heparin Sodium
0641-2460	Heparin Sodium	Heparin Sodium
0641-2450	Heparin Sodium	Heparin Sodium
0781-3327	Heparin Sodium	Heparin Sodium
25021-403	Heparin Sodium	Heparin Sodium
25021-402	Heparin Sodium	Heparin Sodium
25021-400	Heparin Sodium	Heparin Sodium
25021-401	Heparin Sodium	Heparin Sodium
25021-404	Heparin Sodium	Heparin Sodium
48433-329	Heparin Sodium	Heparin Sodium
48433-330	Heparin Sodium	Heparin Sodium
52533-104	Heparin Sodium	Heparin Sodium
52533-125	Heparin Sodium	Heparin Sodium
52533-142	Heparin Sodium	Heparin Sodium
52533-148	Heparin Sodium	Heparin Sodium
52533-211	Heparin Sodium	Heparin Sodium
52533-096	Heparin Sodium	Heparin Sodium
52533-029	Heparin Sodium	Heparin Sodium
52584-540	Heparin Sodium	Heparin Sodium
52533-098	Heparin Sodium	Heparin Sodium
52533-215	Heparin Sodium	Heparin Sodium
52533-097	Heparin Sodium	Heparin Sodium
52533-100	Heparin Sodium	Heparin Sodium
52533-138	Heparin Sodium	Heparin Sodium
52533-106	Heparin Sodium	Heparin Sodium
52533-179	Heparin Sodium	Heparin Sodium
52533-216	Heparin Sodium	Heparin Sodium
52584-400	HEPARIN SODIUM	HEPARIN SODIUM
52584-262	Heparin Sodium	Heparin Sodium
52584-402	Heparin Sodium	Heparin Sodium
52584-542	Heparin Sodium	Heparin Sodium
55154-4749	Heparin Sodium	Heparin Sodium
55154-9354	Heparin Sodium	Heparin Sodium
55154-2827	Heparin Sodium	Heparin Sodium
0338-0424	HEPARIN SODIUM IN SODIUM CHLORIDE	HEPARIN SODIUM
0338-0428	HEPARIN SODIUM IN SODIUM CHLORIDE	HEPARIN SODIUM
0338-0431	HEPARIN SODIUM IN SODIUM CHLORIDE	HEPARIN SODIUM