Potassium Citrate, Sodium Citrate, and Citric Acid
- Product NDC
- 69367-322
- 11-digit product format
- 693670322
- Labeler code
- 69367
- Product ID
- 69367-322_c42a37ea-72e0-499b-a7c5-6557e9d4b613
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Citrate, Sodium Citrate, and Citric Acid Monohydrate
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Westminster Pharmaceuticals, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2021-07-21
- Marketing end
- 0000-00-00
- Substance
- CITRIC ACID MONOHYDRATE; POTASSIUM CITRATE; SODIUM CITRATE, UNSPECIFIED FORM
- Active strength
- 334 mg/5mL; mg/5mL; mg/5mL
- Pharmacologic classes
- Acidifying Activity [MoA], Acidifying Activity [MoA], Acidifying Activity [MoA], Anti-coagulant [EPC], Anti-coagulant [EPC], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calcium Chelating Activity [MoA], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Calculi Dissolution Agent [EPC], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE], Decreased Coagulation Factor Activity [PE], Decreased Coagulation Factor Activity [PE]
- 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 |
|---|
| 69367-322-16 | 69367032216 | 473 mL in 1 BOTTLE (69367-322-16) | 473 ml | 2021-07-21 | 0000-00-00 | No | No | Current |