01 4AMINOPHYLLINE
02 1AMMONIUM CHLORIDE
03 1ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE
04 3CELECOXIB
05 3CLORAZEPATE DIPOTASSIUM
06 2COPPER
07 4ETHINYL ESTRADIOL; ETHYNODIOL DIACETATE
08 1ETHINYL ESTRADIOL;NORETHINDRONE; FERROUS FUMARATE
09 3ETHYNODIOL DIACETATE; MESTRANOL
10 2LIDOCAINE HYDROCHLORIDE
11 2MESTRANOL; NORETHINDRONE
12 5MESTRANOL; NORETHYNODREL
13 2METARAMINOL BITARTRATE
14 3METOLAZONE
15 6POTASSIUM CHLORIDE
16 2PROCAINE HYDROCHLORIDE
17 1PROPANTHELINE BROMIDE
18 1VERAPAMIL HYDROCHLORIDE
01 6CAPSULE;ORAL
02 17INJECTABLE;INJECTION
03 2INTRAUTERINE DEVICE;INTRAUTERINE
04 1SOLUTION;ORAL
05 8TABLET;ORAL
06 3TABLET;ORAL-20
07 5TABLET;ORAL-21
08 4TABLET;ORAL-28
01 10.025MG/5ML;2.5MG/5ML
02 10.035MG;0.5MG;75MG
03 20.035MG;1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
04 10.05MG;1MG
05 10.05MG;1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
06 20.075MG;5MG
07 20.08MG;1MG
08 10.15MG;9.85MG
09 20.1MG;2.5MG
10 21%
11 2100MG
12 110MG
13 1120MG
14 115MG
15 11MEQ/ML
16 31MG;0.1MG
17 22%
18 12.5MG
19 12.5MG/ML
20 2200MG
21 225MG/ML
22 22MEQ/ML
23 13.75MG
24 130MG/VIAL
25 33MEQ/ML
26 1400MG
27 14MEQ/ML
28 15MG
29 17.5MG
30 189MG
31 1EQ 10MG BASE/ML
32 1EQ 20MG BASE/ML
01 42DISCN
02 4Blank
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : AMINOPHYLLIN
Dosage Strength : 100MG
Approval Date : 1982-01-01
Application Number : 2386
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : AMINOPHYLLIN
Dosage Strength : 200MG
Approval Date : 1982-01-01
Application Number : 2386
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : AMINOPHYLLIN
Dosage Strength : 25MG/ML
Approval Date : 1982-05-24
Application Number : 87243
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : AMINOPHYLLIN
Dosage Strength : 25MG/ML
Approval Date : 1982-05-24
Application Number : 87621
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : AMMONIUM CHLORIDE
Dosage Strength : 3MEQ/ML
Approval Date : 1982-01-01
Application Number : 86205
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE
Dosage Form : SOLUTION; ORAL
Proprietary Name : LOMOTIL
Dosage Strength : 0.025MG/5ML;2.5MG/5ML
Approval Date : 1982-01-01
Application Number : 12699
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD :
TE Code :
Dosage Form : CAPSULE; ORAL
Proprietary Name : CELEBREX
Dosage Strength : 100MG
Approval Date :
Application Number : 21156
RX/OTC/DISCN :
RLD :
TE Code :
RLD :
TE Code :
Dosage Form : CAPSULE; ORAL
Proprietary Name : CELEBREX
Dosage Strength : 200MG
Approval Date :
Application Number : 21156
RX/OTC/DISCN :
RLD :
TE Code :
RLD :
TE Code :
Dosage Form : CAPSULE; ORAL
Proprietary Name : CELEBREX
Dosage Strength : 400MG
Approval Date :
Application Number : 21156
RX/OTC/DISCN :
RLD :
TE Code :
RLD : No
TE Code :
Dosage Form : CAPSULE; ORAL
Proprietary Name : CLORAZEPATE DIPOTASSIUM
Dosage Strength : 3.75MG
Approval Date : 1987-12-18
Application Number : 71727
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
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