Formulation Development and Evaluation of Moxifloxacin.HCL Fast Dissolving Tablets.
- Published in:
- Pharmaceutical Methods, 2017, v. 8, n. 2, p. 160, doi. 10.5530/phm.2017.8.24
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- Publication type:
- Article
Works matching IS 22294708 AND DT 2017 AND VI 8 AND IP 2
Results: 13
1
2
An Inclusive Review on Analytical Methods for Ritonavir in Various Pharmaceutical and Biological Matrix.
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- Pharmaceutical Methods, 2017, v. 8, n. 2, p. 149, doi. 10.5530/phm.2017.8.23
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- Publication type:
- Article
3
Preparation of Transdermal Films of Nifedipine: Ex-vivo and In-vitro Studies.
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- Pharmaceutical Methods, 2017, v. 8, n. 2, p. 144, doi. 10.5530/phm.2017.8.22
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- Publication type:
- Article
4
Aggrandizing Delivery of Nalidixic Acid to Colon Employing A Targeted Prodrug Approach: Synthesis and in vivo Evaluation.
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- Pharmaceutical Methods, 2017, v. 8, n. 2, p. 136, doi. 10.5530/phm.2017.8.21
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- Publication type:
- Article
5
Dissolution Modulating Mechanism of Flurbiprofen Solid Dispersions: Characterization, Physical Stability and in vivo Performance: Formulation Considerations and optimization study.
- Published in:
- Pharmaceutical Methods, 2017, v. 8, n. 2, p. 127, doi. 10.5530/phm.2017.8.20
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- Publication type:
- Article
6
Stability Indicating UV Spectrophotometric Method For Linagliptin and Metformin in Pharmaceutical Dosage Form.
- Published in:
- Pharmaceutical Methods, 2017, v. 8, n. 2, p. 121, doi. 10.5530/phm.2017.8.19
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- Publication type:
- Article
7
Fabrication of Extended Release Tablets of Pramipexole: In-vitro Studies.
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- Pharmaceutical Methods, 2017, v. 8, n. 2, p. 115, doi. 10.5530/phm.2017.8.18
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- Publication type:
- Article
8
Modification in the Approach of Developing Solid Dispersed Particles for Enhanced Dissolution.
- Published in:
- Pharmaceutical Methods, 2017, v. 8, n. 2, p. 108, doi. 10.5530/phm.2017.8.17
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- Publication type:
- Article
9
Estimation of Dapagliflozin from its Tablet Formulation by UV-Spectrophotometry.
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- Pharmaceutical Methods, 2017, v. 8, n. 2, p. 102, doi. 10.5530/phm.2017.8.16
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- Publication type:
- Article
10
Quality-By-Design Approach to Stability Indicating RP-HPLC Analytical Method Development for Estimation of Canagliflozin API and Its Validation.
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- Pharmaceutical Methods, 2017, v. 8, n. 2, p. 92, doi. 10.5530/phm.2017.8.15
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- Publication type:
- Article
11
Validated Stability-indicating NP-HPTLC/Densitometry Method for the Assay of Zolpidem Tartrate in Pharmaceutical Dosage Form.
- Published in:
- Pharmaceutical Methods, 2017, v. 8, n. 2, p. 87, doi. 10.5530/phm.2017.8.14
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- Publication type:
- Article
12
Synthesis and Evaluation of Antipsychotic Compounds from Lupeol.
- Published in:
- Pharmaceutical Methods, 2017, v. 8, n. 2, p. 81, doi. 10.5530/phm.2017.8.13
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- Publication type:
- Article
13
Preparation and Evaluation of Sustained Release Colon Targeted Micropellets of Lornoxicam.
- Published in:
- Pharmaceutical Methods, 2017, v. 8, n. 2, p. 75, doi. 10.5530/phm.2017.8.12
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- Publication type:
- Article