sodium chloride
- Product NDC
- 65044-7133
- 11-digit product format
- 650447133
- Labeler code
- 65044
- Product ID
- 65044-7133_64dfd25b-ed5f-4250-a950-921d25edec8d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- sodium chloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Jubilant HollisterStier LLC
- Application
- ANDA203352
- Marketing category
- ANDA
- Marketing start
- 2016-02-29
- Marketing end
- 2021-06-30
- Substance
- SODIUM CHLORIDE
- Active strength
- 9 mg/mL
- Pharmacologic classes
- Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 65044-7133-2 | 65044713302 | 25 VIAL, GLASS in 1 CARTON (65044-7133-2) > 10 mL in 1 VIAL, GLASS (65044-7133-1) | 2016-02-29 | 2021-06-30 | No | No | Current |