METHOCARBAMOL
- Product NDC
- 17511-505
- 11-digit product format
- 175110505
- Labeler code
- 17511
- Product ID
- 17511-505_0d36c94b-24fb-4b04-ab81-6dd2d0bf5557
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METHOCARBAMOL
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- RA CHEM PHARMA LIMITED
- Application
- ANDA203550
- Marketing category
- ANDA
- Marketing start
- 2017-02-08
- Marketing end
- 0000-00-00
- Substance
- METHOCARBAMOL
- Active strength
- 500 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 17511-505-01 | METHOCARBAMOL | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 2 |
| 17511-505-05 | METHOCARBAMOL | 500 in 1 BOTTLE | TABLET, FILM COATED | 500 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17511-505 | METHOCARBAMOL TABLET, FILM COATED [RA CHEM PHARMA LIMITED] | 2 | Legacy NDC, 2 package rows | 20181207_851e7eba-a919-4745-88c8-3e27b2adf319.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 17511-505-01 | 17511050501 | 100 in 1 BOTTLE | Historical |
| 17511-505-05 | 17511050505 | 500 in 1 BOTTLE | Historical |