Tanlor
- Product NDC
- 72245-873
- 11-digit product format
- 722450873
- Labeler code
- 72245
- Product ID
- 72245-873_1dd5eca2-4ad3-5c03-e063-6394a90aa9b0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Forte Bio-Pharma
- Application
- ANDA212707
- Marketing category
- ANDA
- Marketing start
- 2024-08-30
- Substance
- METHOCARBAMOL
- Active strength
- 1000 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Tanlor
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| METHOCARBAMOL | 1000 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 125OD7737X |
| Rxcui | 2611794, 2691000 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72245-873-10 | Tanlor | 100 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 100 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72245-873 | TANLOR (METHOCARBAMOL) TABLET, FILM COATED [FORTE BIO-PHARMA] | 1 | Current NDC, 1 package rows | 20240830_1dd5f7fd-7b3b-8669-e063-6394a90abe95.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72245-873-10 | 72245087310 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72245-873-10) | 2024-08-30 | No | No | Historical |