L-Cysteine Hydrochloride
- Product NDC
- 0781-8940
- 11-digit product format
- 007818940
- Labeler code
- 0781
- Product ID
- 0781-8940_eb92386f-e8ce-4ec3-ad11-8cb57f7b9678
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- L-Cysteine Hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Sandoz Inc
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2016-06-14
- Marketing end
- 2021-06-30
- Substance
- CYSTEINE HYDROCHLORIDE
- Active strength
- 50 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0781-8940-95 | 00781894095 | 10 VIAL, SINGLE-DOSE in 1 CARTON (0781-8940-95) > 10 mL in 1 VIAL, SINGLE-DOSE (0781-8940-70) | 2016-06-14 | 2021-06-30 | No | No | Current |