Phytonadione
- Product NDC
- 60687-600
- 11-digit product format
- 606870600
- Labeler code
- 60687
- Product ID
- 60687-600_c3c941f2-37db-9292-e053-2a95a90a7eff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phytonadione
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA210189
- Marketing category
- ANDA
- Marketing start
- 2021-05-01
- 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 |
|---|
| 60687-600-94 | 60687060094 | 20 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-600-94) > 1 TABLET in 1 BLISTER PACK (60687-600-11) | 20 blister pack | 2021-05-01 | 0000-00-00 | No | No | Current |