Orphenadrine Citrate
- Product NDC
- 67296-0709
- 11-digit product format
- 672960709
- Labeler code
- 67296
- Product ID
- 67296-0709_d5fc2e9d-59d9-29cd-e053-2a95a90afa52
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Orphenadrine Citrate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA040284
- Marketing category
- ANDA
- Marketing start
- 1998-06-19
- Marketing end
- 0000-00-00
- Substance
- ORPHENADRINE CITRATE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67296-0709-1 | Orphenadrine Citrate | 20 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 20 | | 4 |
| 67296-0709-2 | Orphenadrine Citrate | 10 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 10 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-0709 | ORPHENADRINE CITRATE TABLET, EXTENDED RELEASE [REDPHARM DRUG, INC.] | 4 | Legacy NDC, 2 package rows | 20240712_41605713-726c-5a57-e054-00144ff88e88.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67296-0709-1 | 67296070901 | 20 TABLET, EXTENDED RELEASE in 1 BOTTLE (67296-0709-1) | 1998-06-19 | 0000-00-00 | No | No | Current |
| 67296-0709-2 | 67296070902 | 10 in 1 BOTTLE | | | | | Historical |