Diluent
- Product NDC
- 0173-0518
- 11-digit product format
- 001730518
- Labeler code
- 0173
- Product ID
- 0173-0518_22cfe99c-d3ad-4877-9b8f-53c25282fae8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- water
- Dosage form
- SOLUTION
- Route
- INTRAVENOUS
- Labeler
- GlaxoSmithKline LLC
- Application
- NDA020444
- Marketing category
- NDA
- Marketing start
- 2003-05-06
- Marketing end
- 2021-02-14
- Substance
- WATER
- Active strength
- 1 mL/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0173-0518-01 | ML - Milliliter | 0173-0518 | 515cc15b-a1ae-4b57-aad0-07487c844342 | 1 | 2012-07-24 |