NDC 70518-1214

Cryselle

Norgestrel And Ethinyl Estradiol

Cryselle is a Kit in the Human Prescription Drug category. It is labeled and distributed by Remedyrepack Inc.. The primary component is .

• Product ID: 70518-1214_6cbe57f7-0db3-58a3-e053-2a91aa0aa871
• NDC: 70518-1214
• Product Type: Human Prescription Drug
• Proprietary Name: Cryselle
• Generic Name: Norgestrel And Ethinyl Estradiol
• Dosage Form: Kit
• Marketing Start Date: 2018-05-17
• Marketing Category: ANDA / ANDA
• Application Number: ANDA075840
• Labeler Name: REMEDYREPACK INC.
• Active Ingredient Strength: 0
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 70518-1214-0

6 POUCH in 1 CARTON (70518-1214-0) > 1 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK

• Marketing Start Date: 2018-05-17
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 70518-1214-0 [70518121400]

Cryselle KIT

• Marketing Category: ANDA
• Application Number: ANDA075840
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2018-05-17
• Marketing End Date: 2020-03-27
• Inactivation Date: 2020-01-31
• Reactivation Date: 2020-03-27

Drug Details

OpenFDA Data

• SPL SET ID: f92aae3d-d0ba-4911-a479-0fb11a5c08f3
• Manufacturer:
  • REMEDYREPACK INC.
• RxNorm Concept Unique ID - RxCUI:
  • 311359
  • 748797
  • 750265
  • 749786

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

NDC	Brand Name	Generic Name
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
52544-848	Ogestrel	Norgestrel and Ethinyl Estradiol