Meperidine Hydrochloride
- Product NDC
- 0555-0392
- 11-digit product format
- 005550392
- Labeler code
- 0555
- Product ID
- 0555-0392_775057a5-3532-4daf-82f2-67bf46575085
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meperidine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA088640
- Marketing category
- ANDA
- Marketing start
- 2015-02-24
- Marketing end
- 2021-02-28
- Substance
- MEPERIDINE HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- DEA schedule
- CII
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0555-0392-02 | 00555039202 | 100 TABLET in 1 BOTTLE (0555-0392-02) | 100 tablet | 2015-02-24 | 2021-02-28 | No | No | Current |