NDC 0023-5869

Femring

Estradiol Acetate

Femring is a Vaginal Ring in the Human Prescription Drug category. It is labeled and distributed by Allergan, Inc.. The primary component is Estradiol Acetate.

• Product ID: 0023-5869_b08979c2-5940-48df-b455-d3b2ca68d74d
• NDC: 0023-5869
• Product Type: Human Prescription Drug
• Proprietary Name: Femring
• Generic Name: Estradiol Acetate
• Dosage Form: Ring
• Route of Administration: VAGINAL
• Marketing Start Date: 2016-05-02
• Marketing End Date: 2020-05-31
• Marketing Category: NDA / NDA
• Application Number: NDA021367
• Labeler Name: Allergan, Inc.
• Substance Name: ESTRADIOL ACETATE
• Active Ingredient Strength: 0 mg/d
• Pharm Classes: Estradiol Congeners [CS],Estrogen [EPC],Estrogen Receptor Agonists [MoA]
• NDC Exclude Flag: N

Packaging

NDC 0023-5869-10

1 POUCH in 1 CARTON (0023-5869-10) > 90 d in 1 POUCH

• Marketing Start Date: 2016-05-02
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0023-5869-10 [00023586910]

Femring RING

• Marketing Category: NDA
• Application Number: NDA021367
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2016-05-02
• Marketing End Date: 2020-05-31

Drug Details

Active Ingredients

Ingredient	Strength
ESTRADIOL ACETATE	.1 mg/d

OpenFDA Data

• SPL SET ID: 9e4c5295-1fe9-4da3-90f9-04204e3e72e4
• Manufacturer:
  • Allergan, Inc.
• UNII:
  • 5R97F5H93P
• RxNorm Concept Unique ID - RxCUI:
  • 848342
  • 848331
  • 848343
  • 848333

Pharmacological Class

• Estradiol Congeners [CS]
• Estrogen [EPC]
• Estrogen Receptor Agonists [MoA]
• Estradiol Congeners [CS]
• Estrogen [EPC]
• Estrogen Receptor Agonists [MoA]

NDC Crossover Matching brand name "Femring" or generic name "Estradiol Acetate"

NDC	Brand Name	Generic Name
0023-5868	Femring	estradiol acetate
0023-5869	Femring	estradiol acetate
72495-201	Femring	estradiol acetate
72495-202	Femring	estradiol acetate