Search by Drug Name or NDC
NDC 72789-0022-98 Methocarbamol 750 mg/1 Details
Methocarbamol 750 mg/1
Methocarbamol is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PD-Rx Pharmaceuticals, Inc.. The primary component is METHOCARBAMOL.
Product Information
| NDC | 72789-0022 |
|---|---|
| Product ID | 72789-022_0a1f2eba-4119-82ae-e063-6394a90a4b27 |
| Associated GPIs | 75100070000310 |
| GCN Sequence Number | 004655 |
| GCN Sequence Number Description | methocarbamol TABLET 750 MG ORAL |
| HIC3 | H6H |
| HIC3 Description | SKELETAL MUSCLE RELAXANTS |
| GCN | 17893 |
| HICL Sequence Number | 001938 |
| HICL Sequence Number Description | METHOCARBAMOL |
| Brand/Generic | Generic |
| Proprietary Name | Methocarbamol |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Methocarbamol |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 750 |
| Active Ingredient Units | mg/1 |
| Substance Name | METHOCARBAMOL |
| Labeler Name | PD-Rx Pharmaceuticals, Inc. |
| Pharmaceutical Class | Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA208507 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 72789-0022-98 (72789002298)
| NDC Package Code | 72789-022-98 |
|---|---|
| Billing NDC | 72789002298 |
| Package | 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-98) |
| Marketing Start Date | 2023-09-12 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |