Phytonadione
- Product NDC
- 68682-170
- 11-digit product format
- 686820170
- Labeler code
- 68682
- Product ID
- 68682-170_f926a516-058f-434f-a2bf-f024c6f63566
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- phytonadione
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Oceanside Pharmaceuticals
- Application
- NDA010104
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2018-04-23
- 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
- 2023-12-31
- 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 |
|---|
| 68682-170-30 | 68682017030 | 1 BOTTLE in 1 CARTON (68682-170-30) > 30 TABLET in 1 BOTTLE | 1 bottle | 2018-04-23 | 0000-00-00 | No | No | Current |