Unique Ingredient Identifier XF417D3PSL is listed as a ingredient substance
RN | 77-92-9 |
EC | 201-069-1 |
NCIT | C80088 |
RXCUI | 221946 |
PUBCHEM | 311 |
MF | C6H8O7 |
INCHI KEY | KRKNYBCHXYNGOX-UHFFFAOYSA-N |
SMILES | OC(=O)CC(O)(CC(O)=O)C(O)=O |
UNII XF417D3PSL ANHYDROUS CITRIC ACID is commonly included in medications in the following forms.
Route | Dosage Form | Potency |
---|---|---|
BUCCAL | FILM | 1.04 MG |
IM - IV | INJECTION | 0.33 % |
INHALATION | SUSPENSION | 0.56 mg/2mL |
INTRACARDIAC | INJECTION | 12.5 mg/5mL |
INTRAMUSCULAR | INJECTION | 12.5 mg/5mL |
INTRAMUSCULAR | INJECTION | 0.2 %W/V |
INTRAMUSCULAR | INJECTION, SOLUTION | 0.25 % |
INTRAVENOUS | INJECTABLE | 0.2 % |
INTRAVENOUS | INJECTION | 10 MG/1ML |
INTRAVENOUS | INJECTION | 7.7 %W/V |
INTRAVENOUS | INJECTION, SOLUTION | 0.4 %W/V |
INTRAVENOUS | LIQUID | 2 MG/1ML |
INTRAVENOUS | LIQUID | 0.2 % |
INTRAVENOUS | POWDER, FOR INJECTION SOLUTION, LYOPHILIZED | 42.19 % |
INTRAVENOUS | SOLUTION, INJECTION | 1 % |
INTRAVENOUS | SOLUTION, INJECTION | 0.14 ADJ PH |
INTRAVENOUS INFUSION | INJECTION | 4 MG/1ML |
INTRAVENOUS INFUSION | SOLUTION, INJECTION | 0.53 % |
INTRAVENOUS INFUSION | SOLUTION, INJECTION | 0.025 mg/mL |
IV(INFUSION) | INJECTABLE | 7.7 %W/V |
IV(INFUSION) | SOLUTION, CONCENTRATE | 0.6 % |
IV(INFUSION) | SOLUTION, INJECTION | 1 % |
NASAL | SOLUTION, SPRAY | 0.044 % |
NASAL | SPRAY | 0.058 % |
NASAL | SPRAY, METERED | 0.045 % |
OPHTHALMIC | SOLUTION | 0.93 MG/1ML |
ORAL | CAPSULE, SOFT GELATIN | 1.64 MG |
ORAL | CAPSULE, SOFT GELATIN LIQUID-FILLED | 30 MG |
ORAL | GRANULE, FOR ORAL SUSPENSION | 4.9 MG |
ORAL | LIQUID | 2 MG/1ML |
ORAL | LIQUID | 2 mg/10mL |
ORAL | LIQUID,EXTENDED RELEASE | 5.18 MG/ML |
ORAL | POWDER, FOR ORAL SOLUTION | 210 MG |
ORAL | POWDER, FOR ORAL SUSPENSION | 100 mg |
ORAL | POWDER, FOR ORAL SUSPENSION | 60 MG/PKT |
ORAL | POWDER, FOR SOLUTION | 7.99 MG |
ORAL | POWDER, FOR SUSPENSION | 10 MG/140ML |
ORAL | SOLUTION | 33.18 MG/5ML |
ORAL | SOLUTION | 15 mg/5 mL |
ORAL | SOLUTION | 0.675 mg/15 mL |
ORAL | SOLUTION | ADJ PH |
ORAL | SOLUTION, ELIXIR | 5 MG/5ML |
ORAL | SOLUTION, LIQUID | 0.8 MG/1ML |
ORAL | SUSPENSION | 75 MG/5ML |
ORAL | SUSPENSION | 5.1 MG/5 ML |
ORAL | SUSPENSION | 4.9 mg/1mL |
ORAL | SUSPENSION | 2.25 mg/1.25mL |
ORAL | SUSPENSION, DROPS | 2.5 MG/1ML |
ORAL | SUSPENSION, EXTENDED RELEASE | 2.25 MG/1ML |
ORAL | SYRUP | 22.32 MG/5ML |
ORAL | SYRUP | 0.7 MG/ML |
ORAL | TABLET | 20.4 MG |
ORAL | TABLET | ADJ PH |
ORAL | TABLET, CHEWABLE | 8 MG |
ORAL | TABLET, EFFERVESCENT, FOR SOLUTION | 839.63 MG |
ORAL | TABLET, EXTENDED RELEASE | 78 MG |
ORAL | TABLET, ORALLY DISINTEGRATING | 30 MG |
ORAL | TABLET, ORALLY DISINTEGRATING | ADJ PH |
ORAL | TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE | 8 mg |
ORAL | TABLET, UNCOATED, LOZENGE | 9.8 MG |
RECTAL | SUSPENSION | 0.11 % |
RESPIRATORY (INHALATION) | SOLUTION, SPRAY | 0.0003 % |
RESPIRATORY (INHALATION) | SUSPENSION, FOR INHALATION | 0.027 % |
SUBCUTANEOUS | INJECTION | 12.5 mg/5mL |
SUBCUTANEOUS | INJECTION | 0.2 % |
SUBCUTANEOUS | INJECTION, SOLUTION | 0.25 % |
SUBLINGUAL | FILM | 5.56 mg |
SUBLINGUAL | TABLET | 10 MG |
SUBLINGUAL | TABLET (IMMED./COMP. RELEASE), UNCOATED, BUCCAL | 6 MG |
SUBLINGUAL | TABLET, ORALLY DISINTEGRATING | ADJ PH |
TOPICAL | AEROSOL | 0.01 %W/W |
TOPICAL | AEROSOL, FOAM | ADJPH |
TOPICAL | AEROSOL, FOAM | ADJ PH |
TOPICAL | CLOTH | 0.15 %W/W |
TOPICAL | CREAM | 0.05 %W/W |
TOPICAL | CREAM | 0.01 %W/W |
TOPICAL | CREAM, EMULSION, SUSTAINED RELEASE | 0.18 %W/W |
TOPICAL | EMULSION, AEROSOL FOAM | 0.08 %W/W |
TOPICAL | EMULSION, CREAM | 0.05 %W/W |
TOPICAL | GEL | 0.05 %W/W |
TOPICAL | LOTION | 0.42 %W/W |
TOPICAL | OIL | 0.03 %W/W |
TOPICAL | OPHTHALMIC SUSPENSION DOSAGE FORM | 0.05 %W/V |
TOPICAL | SOLUTION | 0.93 MG/1ML |
TOPICAL | SOLUTION | 0.2 %W/W |
TRANSDERMAL | PATCH, ELECTRICALLY CONTROLLED | 23 MG |
TRANSMUCOSAL | TABLET, UNCOATED, LOZENGE | 11 MG |