Caffeine Citrate
- Product NDC
- 0517-0020
- 11-digit product format
- 005170020
- Labeler code
- 0517
- Product ID
- 0517-0020_7daa7474-b04e-4ffe-a75d-30ee0a83baaa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Caffeine Citrate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- American Regent, Inc.
- Application
- ANDA077906
- Marketing category
- ANDA
- Marketing start
- 2007-09-10
- Marketing end
- 0000-00-00
- Substance
- CAFFEINE CITRATE
- Active strength
- 20 mg/mL
- Pharmacologic classes
- Central Nervous System Stimulant [EPC],Methylxanthine [EPC],Xanthines [CS],Central Nervous System Stimulation [PE]
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0517-0020-10 | 00517002010 | 10 VIAL, SINGLE-DOSE in 1 BOX (0517-0020-10) > 3 mL in 1 VIAL, SINGLE-DOSE | 2007-09-10 | 0000-00-00 | No | No | Current |
| 0517-0020-25 | 00517002025 | 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-0020-25) > 3 mL in 1 VIAL, SINGLE-DOSE | 2007-09-10 | 0000-00-00 | No | No | Current |