Phytonadione
- Product NDC
- 52565-142
- 11-digit product format
- 525650142
- Labeler code
- 52565
- Product ID
- 52565-142_b613e06c-a234-48eb-84f0-f85923a15a9e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- phytonadione
- Dosage form
- INJECTION, EMULSION
- Route
- INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
- Labeler
- Teligent Pharma, Inc.
- Application
- NDA012223
- Marketing category
- NDA
- Marketing start
- 2018-03-07
- Marketing end
- 0000-00-00
- Substance
- PHYTONADIONE
- Active strength
- 2 mg/mL
- Pharmacologic classes
- Increased Prothrombin Activity [PE],Reversed Anticoagulation Activity [PE],Vitamin K [CS],Vitamin K [EPC],Warfarin Reversal Agent [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record