atovaquone
- Product NDC
- 16714-900
- 11-digit product format
- 167140900
- Labeler code
- 16714
- Product ID
- 16714-900_01647cef-3e92-4724-a814-c2a0a246bf27
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- atovaquone
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Northstar Rx LLC
- Application
- ANDA209685
- Marketing category
- ANDA
- Marketing start
- 2019-03-01
- Marketing end
- 0000-00-00
- Substance
- ATOVAQUONE
- Active strength
- 750 mg/5mL
- Pharmacologic classes
- Antimalarial [EPC],Antiprotozoal [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 16714-900-01 | 16714090001 | 210 mL in 1 BOTTLE (16714-900-01) | 210 ml | 2019-03-01 | 0000-00-00 | No | No | Current |