Pseudoephedrine Hydrochloride
- Product NDC
- 70518-2318
- 11-digit product format
- 705182318
- Labeler code
- 70518
- Product ID
- 70518-2318_c832a1a5-fa1e-d508-e053-2a95a90a61ba
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Pseudoephedrine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2019-09-19
- Marketing end
- 0000-00-00
- Substance
- PSEUDOEPHEDRINE HYDROCHLORIDE
- Active strength
- 60 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2318-0 | 70518231800 | 20 TABLET in 1 BOTTLE, PLASTIC (70518-2318-0) | 20 tablet | 2019-09-19 | 0000-00-00 | No | No | Current |