ROBAXIN
- Product NDC
- 61919-354
- 11-digit product format
- 619190354
- Labeler code
- 61919
- Product ID
- 61919-354_33209430-6d78-1c13-e054-00144ff8d46c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METHOCARBAMOL
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA200958
- Marketing category
- ANDA
- Marketing start
- 2016-02-03
- Marketing end
- 0000-00-00
- Substance
- METHOCARBAMOL
- Active strength
- 750 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 61919-354-40 | ROBAXIN | 1 in 1 BOTTLE | TABLET, FILM COATED | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-354 | ROBAXIN (METHOCARBAMOL) TABLET, FILM COATED [DIRECT RX] | 1 | Legacy NDC, 1 package rows | 20160518_33209430-6d77-1c13-e054-00144ff8d46c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 61919-354-40 | 61919035440 | 1 in 1 BOTTLE | Historical |