Download:
pdf |
pdf[Company]
A
AG Trade
Name, if any
AG Drugs and Information
B
Brand-Name
C
Active Ingredient
D
Dosage
Form
E
NDA #
1
FTC Authorized Generic Drug Study
Page 1 of 2
F
G
H
Dosage 14-digit Generic AG's 9 digit
Strength Product Identifier
NDC #
(Labeler
Code Product
Code)
Questions 4, 5
I
Labeler/Entity Name
OMB Control No. [insert]
[Company]
1
H
AG's 9 digit
NDC #
(Labeler
Code Product
Code)
AG Drugs and Information
J
Date of Launch
FTC Authorized Generic Drug Study
Questions 4, 5
K
L
Date of first
Date of
Discontinuance, if announcement of
AG marketing
any
Page 2 of 2
OMB Control No. [insert]
File Type | application/pdf |
File Title | Example-FTC provides SO to AG 4-25-blank.xls |
File Modified | 2007-05-04 |
File Created | 2007-05-04 |