NDC 52544-848

Ogestrel

Norgestrel And Ethinyl Estradiol

Ogestrel is a Kit in the Human Prescription Drug category. It is labeled and distributed by Actavis Pharma, Inc.. The primary component is .

• Product ID: 52544-848_04dfe658-5e97-4c06-96d8-6f3eb0061f57
• NDC: 52544-848
• Product Type: Human Prescription Drug
• Proprietary Name: Ogestrel
• Generic Name: Norgestrel And Ethinyl Estradiol
• Dosage Form: Kit
• Marketing Start Date: 2000-08-21
• Marketing End Date: 2020-11-30
• Marketing Category: ANDA / ANDA
• Application Number: ANDA075406
• Labeler Name: Actavis Pharma, Inc.
• Active Ingredient Strength: 0
• NDC Exclude Flag: N

Packaging

NDC 52544-848-28

3 BLISTER PACK in 1 CARTON (52544-848-28) > 1 KIT in 1 BLISTER PACK

• Marketing Start Date: 2000-08-21
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 52544-848-28 [52544084828]

Ogestrel KIT

• Marketing Category: ANDA
• Application Number: ANDA075406
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2000-08-21
• Marketing End Date: 2020-11-30

Drug Details

OpenFDA Data

• SPL SET ID: 90b9421c-5865-43c5-a984-49351e1f20a1
• Manufacturer:
  • Actavis Pharma, Inc.
• RxNorm Concept Unique ID - RxCUI:
  • 748797
  • 314146
  • 750242
  • 750243

Medicade Reported Pricing

52544084828 OGESTREL TABLET

Pricing Unit: EA | Drug Type:

NDC Crossover Matching brand name "Ogestrel" or generic name "Norgestrel And Ethinyl Estradiol"

NDC	Brand Name	Generic Name
52544-848	Ogestrel	Norgestrel and Ethinyl Estradiol
0555-9049	Cryselle	Norgestrel and Ethinyl Estradiol
50090-2183	Cryselle	Norgestrel and Ethinyl Estradiol
53002-1188	Cryselle	Norgestrel and Ethinyl Estradiol
70518-1214	Cryselle	Norgestrel and Ethinyl Estradiol
16714-365	Elinest	Norgestrel and Ethinyl Estradiol
51862-564	Low-Ogestrel	Norgestrel and Ethinyl Estradiol
53002-1637	Low-Ogestrel	Norgestrel and Ethinyl Estradiol