meperidine hydrochloride
- Product NDC
- 46672-831
- 11-digit product format
- 466720831
- Labeler code
- 46672
- Product ID
- 46672-831_9c56afa2-bfa0-fa03-e053-2995a90a7437
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- meperidine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mikart, LLC
- Application
- ANDA040893
- Marketing category
- ANDA
- Marketing start
- 2009-06-24
- Marketing end
- 0000-00-00
- 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
- 2021-12-31
- 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 |
|---|
| 46672-831-10 | 46672083110 | 100 TABLET in 1 BOTTLE, PLASTIC (46672-831-10) | 100 tablet | 2009-06-24 | 0000-00-00 | No | No | Current |
| 46672-831-50 | 46672083150 | 500 TABLET in 1 BOTTLE, PLASTIC (46672-831-50) | 500 tablet | 2009-06-24 | 0000-00-00 | No | No | Current |