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01 3ABBVIE
02 1DR REDDYS LABS SA
03 1STRIDES PHARMA
04 1MANKIND PHARMA
05 1ABLE
06 6ACCORD HLTHCARE
07 1ALCON LABS INC
08 1ALPHARMA US PHARMS
09 2AM REGENT
10 3AMNEAL
11 1ANI PHARMS
12 1APOTEX
13 1ASCOT
14 1BAUSCH AND LOMB INC
15 1CHARTWELL RX
16 2FOSUN PHARMA
17 1FRESENIUS KABI USA
18 1GD SEARLE LLC
19 1HALSEY
20 1HEATHER
21 3HIKMA
22 3HOSPIRA
23 1INTL MEDICATION SYS
24 1INWOOD LABS
25 1KV PHARM
26 1LANNETT
27 1LEADING
28 1LEDERLE
29 2LEGACY PHARMA
30 1MD PHARM
31 1MEDEFIL INC
32 2MEDPOINTE PHARM HLC
33 2NORVIUM BIOSCIENCE
34 1PARKE DAVIS
35 1PFIZER
36 1PHARMOBEDIENT
37 1PVT FORM
38 1R AND S PHARMA
39 1RISING
40 1ROXANE
41 1SCHERER RP
42 1SOMERSET
43 4SOMERSET THERAPS LLC
44 1SPECGX LLC
45 1SUN PHARM INDUSTRIES
46 1SUPERPHARM
47 1UNICHEM
48 1UPSHER SMITH LABS
49 1US ARMY
50 1USL PHARMA
51 1VALEANT PHARM INTL
52 1VANGARD
53 1WATSON LABS
54 1WINDER LABS LLC
55 3WYETH AYERST
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01 1AEROSOL, METERED;INHALATION
02 1CAPSULE;ORAL
03 8INJECTABLE;INJECTION
04 8SOLUTION/DROPS;OPHTHALMIC
05 16SOLUTION;INTRAVENOUS
06 4SOLUTION;INTRAVENOUS, INTRAMUSCULAR, SUBCUTANEOUS, INTRAOSSEOUS, ENDOT
07 4SOLUTION;ORAL
08 36TABLET;ORAL
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01 41DISCN
02 37RX
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01 3ATROPINE AND DEMEROL
02 28ATROPINE SULFATE
03 2COLONAID
04 1DI-ATRO
05 28DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE
06 1DIPHENOXYLATE HYDROCHLORIDE W/ ATROPINE SULFATE
07 2ENLON-PLUS
08 1ISOPTO ATROPINE
09 1LO-TROL
10 1LOGEN
11 1LOMANATE
12 2LOMOTIL
13 1LONOX
14 1LOW-QUEL
15 3MEPERIDINE AND ATROPINE SULFATE
16 1MOTOFEN
17 1MOTOFEN HALF-STRENGTH
01 66No
02 12Yes
RLD : No
TE Code :
ATROPINE SULFATE; MEPERIDINE HYDROCHLORIDE
Brand Name : ATROPINE AND DEMEROL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 0.4MG/ML;75MG/ML
Approval Date : 1982-11-26
Application Number : 87847
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
RLD : No
TE Code :
ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE
Brand Name : DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE
Dosage Form : TABLET;ORAL
Dosage Strength : 0.025MG;2.5MG
Approval Date : 2020-06-03
Application Number : 210789
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE
Brand Name : DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE
Dosage Form : TABLET;ORAL
Dosage Strength : 0.025MG;2.5MG
Approval Date : 2000-05-02
Application Number : 40357
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
RLD : No
TE Code : AT1
Brand Name : ATROPINE SULFATE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 1%
Approval Date : 2024-01-08
Application Number : 218148
RX/OTC/DISCN : RX
RLD : No
TE Code : AT1
RLD : No
TE Code :
ATROPINE SULFATE; MEPERIDINE HYDROCHLORIDE
Brand Name : ATROPINE AND DEMEROL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 0.4MG/ML;100MG/ML
Approval Date : 1982-11-26
Application Number : 87848
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ATROPINE SULFATE; MEPERIDINE HYDROCHLORIDE
Brand Name : ATROPINE AND DEMEROL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 0.4MG/ML;50MG/ML
Approval Date : 1982-11-26
Application Number : 87853
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE
Brand Name : LOMOTIL
Dosage Form : SOLUTION;ORAL
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 : No
TE Code :
ATROPINE SULFATE; DIFENOXIN HYDROCHLORIDE
Brand Name : MOTOFEN HALF-STRENGTH
Dosage Form : TABLET;ORAL
Dosage Strength : 0.025MG;0.5MG
Approval Date : 1982-01-01
Application Number : 17744
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
ATROPINE SULFATE; DIFENOXIN HYDROCHLORIDE
Brand Name : MOTOFEN
Dosage Form : TABLET;ORAL
Dosage Strength : 0.025MG;1MG
Approval Date : 1982-01-01
Application Number : 17744
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code : AA
ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE
Brand Name : LOMOTIL
Dosage Form : TABLET;ORAL
Dosage Strength : 0.025MG;2.5MG
Approval Date : 1982-01-01
Application Number : 12462
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AA