Progesterone (Page 8 of 8)

PRINCIPAL DISPLAY PANEL — 100 mg Capsule Bottle Label

NDC: 70934-914-30

Label
(click image for full-size original)
PROGESTERONE progesterone capsule
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:70934-914(NDC:70700-162)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PROGESTERONE (PROGESTERONE) PROGESTERONE 100 mg
Inactive Ingredients
Ingredient Name Strength
PEANUT OIL
GELATIN, UNSPECIFIED
GLYCERIN
LECITHIN, SOYBEAN
TITANIUM DIOXIDE
MEDIUM-CHAIN TRIGLYCERIDES
Product Characteristics
Color white (Off-White) Score no score
Shape OVAL Size 12mm
Flavor Imprint Code PR1
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:70934-914-30 30 CAPSULE in 1 BOTTLE, PLASTIC None
2 NDC:70934-914-10 10 CAPSULE in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA205229 10/25/2021
Labeler — Denton Pharma, Inc. DBA Northwind Pharmaceuticals (080355546)
Registrant — Denton Pharma, Inc. DBA Northwind Pharmaceuticals (080355546)
Establishment
Name Address ID/FEI Operations
Denton Pharma, Inc. DBA Northwind Pharmaceuticals 080355546 repack (70934-914)

Revised: 10/2021 Denton Pharma, Inc. DBA Northwind Pharmaceuticals

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