NDC 71700-112

GETTIK Hair Regrowth Treatment

Minoxidil 5%

GETTIK Hair Regrowth Treatment is a Topical Liquid in the Human Otc Drug category. It is labeled and distributed by Gettik International Llc. The primary component is Minoxidil.

• Product ID: 71700-112_61986adc-0d5c-ed88-e053-2991aa0ac90a
• NDC: 71700-112
• Product Type: Human Otc Drug
• Proprietary Name: GETTIK Hair Regrowth Treatment
• Generic Name: Minoxidil 5%
• Dosage Form: Liquid
• Route of Administration: TOPICAL
• Marketing Start Date: 2017-10-01
• Marketing Category: ANDA / ANDA
• Application Number: ANDA074588
• Labeler Name: GETTIK International LLC
• Substance Name: MINOXIDIL
• Active Ingredient Strength: 50 mg/mL
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 71700-112-05

3 BOTTLE, PLASTIC in 1 BOX (71700-112-05) > 60 mL in 1 BOTTLE, PLASTIC

• Marketing Start Date: 2017-10-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 71700-112-05 [71700011205]

GETTIK Hair Regrowth Treatment LIQUID

• Marketing Category: ANDA
• Application Number: ANDA074588
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2017-10-01
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
MINOXIDIL	50 mg/mL

OpenFDA Data

• SPL SET ID: 57dbf5bb-d2b9-4a3a-e053-2a91aa0ae971
• Manufacturer:
  • GETTIK International LLC
• UNII:
  • 5965120SH1
• RxNorm Concept Unique ID - RxCUI:
  • 311724

NDC Crossover Matching brand name "GETTIK Hair Regrowth Treatment" or generic name "Minoxidil 5%"

NDC	Brand Name	Generic Name
71700-112	GETTIK Hair Regrowth Treatment	MINOXIDIL 5%
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