Carisoprodol
- Product NDC
- 50436-0705
- 11-digit product format
- 504360705
- Labeler code
- 50436
- Product ID
- 50436-0705_d165acb8-7475-4e1e-b3f3-ca70cc795f20
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carisoprodol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA205085
- Marketing category
- ANDA
- Marketing start
- 2015-06-01
- Marketing end
- 0000-00-00
- Substance
- CARISOPRODOL
- Active strength
- 350 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50436-0705-1 | Carisoprodol | 30 in 1 BOTTLE | TABLET | 30 | | 7 |
| 50436-0705-2 | Carisoprodol | 60 in 1 BOTTLE | TABLET | 60 | | 7 |
| 50436-0705-3 | Carisoprodol | 90 in 1 BOTTLE | TABLET | 90 | | 7 |
| 50436-0705-4 | Carisoprodol | 120 in 1 BOTTLE | TABLET | 120 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-0705 | CARISOPRODOL TABLET [UNIT DOSE SERVICES] | 7 | Legacy NDC, 4 package rows | 20190813_41c8bf11-001b-4ab7-9e35-c7ad0a0f108e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-0705-1 | 50436070501 | 30 in 1 BOTTLE | Historical |
| 50436-0705-2 | 50436070502 | 60 in 1 BOTTLE | Historical |
| 50436-0705-3 | 50436070503 | 90 in 1 BOTTLE | Historical |
| 50436-0705-4 | 50436070504 | 120 in 1 BOTTLE | Historical |