LIQUIVIDA HYDRATION
- Product NDC
- 49836-031
- 11-digit product format
- 498360031
- Labeler code
- 49836
- Product ID
- 49836-031_a69d3e07-77c4-4b11-a7a4-c95fae071dd3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SODIUM CHLORIDE
- Dosage form
- KIT
- Labeler
- RX PHARMA-PACK, INC.
- Application
- NDA016677
- Marketing category
- NDA
- Marketing start
- 2019-08-05
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 49836-031-04 | EA - Each | 49836-031 | 4195c4a1-a258-404b-a145-a00f5db7a13f | 1 | 2019-08-06 |