Phytonadione
- Product NDC
- 50268-661
- 11-digit product format
- 502680661
- Labeler code
- 50268
- Product ID
- 50268-661_bbb2e2ea-7998-74b7-e053-2a95a90af3e0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- phytonadione
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvPAK
- Application
- NDA010104
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2021-02-19
- Marketing end
- 0000-00-00
- Substance
- PHYTONADIONE
- Active strength
- 5 mg/1
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50268-661-13 | 50268066113 | 30 BLISTER PACK in 1 BOX (50268-661-13) > 1 TABLET in 1 BLISTER PACK (50268-661-11) | 30 blister pack | 2021-02-19 | 0000-00-00 | No | No | Current |