01 9AMPICILLIN SODIUM
02 3AMPICILLIN SODIUM; SULBACTAM SODIUM
03 3CALCIUM GLUCONATE
04 1CEFACLOR
05 1CEFAZOLIN SODIUM
06 1CILASTATIN SODIUM; IMIPENEM
07 4CISPLATIN
08 4DEXMEDETOMIDINE HYDROCHLORIDE
09 4ESMOLOL HYDROCHLORIDE
10 4LEVETIRACETAM
11 2LINEZOLID
12 6MAGNESIUM SULFATE
13 3MEROPENEM
14 1PACLITAXEL
15 3PENICILLIN G POTASSIUM
16 1TENIPOSIDE
01 33HQ SPCLT PHARMA
02 16HQ SPECLT PHARMA
03 1WORLD GEN
01 31INJECTABLE;INJECTION
02 4INJECTABLE;INTRAVENOUS
03 3POWDER;INTRAVENOUS
04 11SOLUTION;INTRAVENOUS
05 1TABLET, EXTENDED RELEASE;ORAL
01 10.5MG/ML
02 11,000,000 UNITS/VIAL
03 11.5GM/100ML (15MG/ML)
04 110MG/ML
05 110MG/VIAL
06 21GM/100ML
07 21GM/100ML (10MG/ML)
08 11GM/50ML (20MG/ML)
09 11GM/VIAL
10 11MG/ML
11 12.5GM/250ML (10MG/ML)
12 120,000,000 UNITS/VIAL
13 1200MG/100ML (2MG/ML)
14 120GM/500ML (40MG/ML)
15 1250MG/50ML (5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
16 12GM/100ML
17 22GM/100ML (20MG/ML)
18 12GM/50ML (40MG/ML)
19 12GM/VIAL
20 140GM/1000ML (40MG/ML)
21 14GM/100ML (40MG/ML)
22 14GM/50ML (80MG/ML)
23 15,000,000 UNITS/VIAL
24 1500MG/100ML (5MG/ML)
25 1500MG/VIAL
26 150MG/VIAL
27 1600MG/300ML (2MG/ML)
28 16MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
29 1EQ 10GM BASE/VIAL
30 1EQ 10GM BASE/VIAL;EQ 5GM BASE/VIAL
31 1EQ 125MG BASE/VIAL
32 2EQ 1GM BASE/VIAL
33 1EQ 1GM BASE/VIAL;EQ 500MG BASE/VIAL
34 1EQ 1MG BASE/10ML (EQ 100MCG BASE/ML)
35 1EQ 200MCG BASE/50ML (EQ 4MCG BASE/ML)
36 1EQ 250MG BASE/VIAL
37 3EQ 2GM BASE/VIAL
38 1EQ 2GM BASE/VIAL;EQ 1GM BASE/VIAL
39 1EQ 400MCG BASE/100ML (EQ 4MCG BASE/ML)
40 1EQ 400MCG BASE/4ML (EQ 100MCG BASE/ML)
41 1EQ 500MG BASE
42 2EQ 500MG BASE/VIAL
43 1EQ 500MG BASE/VIAL;500MG/VIAL
01 50USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : AMPICILLIN SODIUM
Dosage Strength : EQ 1GM BASE/VIAL
Packaging :
Approval Date : 1993-04-15
Application Number : 62772
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : AMPICILLIN SODIUM
Dosage Strength : EQ 1GM BASE/VIAL
Packaging :
Approval Date : 1993-04-15
Application Number : 62772
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : AMPICILLIN SODIUM
Dosage Strength : EQ 2GM BASE/VIAL
Packaging :
Approval Date : 1993-04-15
Application Number : 62772
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : AMPICILLIN SODIUM
Dosage Strength : EQ 2GM BASE/VIAL
Packaging :
Approval Date : 1993-04-15
Application Number : 62772
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : AMPICILLIN SODIUM
Dosage Strength : EQ 125MG BASE/VIAL
Packaging :
Approval Date : 1993-04-15
Application Number : 62772
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : AMPICILLIN SODIUM
Dosage Strength : EQ 250MG BASE/VIAL
Packaging :
Approval Date : 1993-04-15
Application Number : 62772
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : AMPICILLIN SODIUM
Dosage Strength : EQ 500MG BASE/VIAL
Packaging :
Approval Date : 1993-04-15
Application Number : 62772
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : AMPICILLIN SODIUM
Dosage Strength : EQ 500MG BASE/VIAL
Packaging :
Approval Date : 1993-04-15
Application Number : 62772
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : AMPICILLIN SODIUM
Dosage Strength : EQ 10GM BASE/VIAL
Packaging :
Approval Date : 1993-04-15
Application Number : 63142
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Dosage Form : INJECTABLE;INJECTION
Brand Name : AMPICILLIN AND SULBACTAM
Dosage Strength : EQ 2GM BASE/VIAL;EQ 1G...
Packaging :
Approval Date : 2005-11-30
Application Number : 65176
Regulatory Info : RX
Registration Country : USA
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