Relpax
- Product NDC
- 21695-871
- 11-digit product format
- 216950871
- Labeler code
- 21695
- Product ID
- 21695-871_6bb510c8-2ae2-4159-b4c6-0aec5e64b4c9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- eletriptan hydrobromide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Rebel Distributors Corp
- Application
- NDA021016
- Marketing category
- NDA
- Marketing start
- 2002-12-26
- Marketing end
- 0000-00-00
- Substance
- ELETRIPTAN HYDROBROMIDE
- Active strength
- 40 mg/1
- Pharmacologic classes
- Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 21695-871-40 | Relpax | 12 in 1 BLISTER PACK | TABLET, FILM COATED | 12 | | 1 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| eletriptan hydrobromide | ACTIVE INGREDIENT | M41W832TA3 | RELPAX (ELETRIPTAN HYDROBROMIDE) TABLET, FILM COATED [REBEL DISTRIBUTORS CORP] | 1 | |
| eletriptan | ACTIVE MOIETY | 22QOO9B8KI | RELPAX (ELETRIPTAN HYDROBROMIDE) TABLET, FILM COATED [REBEL DISTRIBUTORS CORP] | 1 | |
| Aluminum Oxide | INACTIVE INGREDIENT | LMI26O6933 | RELPAX (ELETRIPTAN HYDROBROMIDE) TABLET, FILM COATED [REBEL DISTRIBUTORS CORP] | 1 | |
| cellulose, microcrystalline | INACTIVE INGREDIENT | OP1R32D61U | RELPAX (ELETRIPTAN HYDROBROMIDE) TABLET, FILM COATED [REBEL DISTRIBUTORS CORP] | 1 | |
| croscarmellose sodium | INACTIVE INGREDIENT | M28OL1HH48 | RELPAX (ELETRIPTAN HYDROBROMIDE) TABLET, FILM COATED [REBEL DISTRIBUTORS CORP] | 1 | |
| FD&C YELLOW NO. 6 | INACTIVE INGREDIENT | H77VEI93A8 | RELPAX (ELETRIPTAN HYDROBROMIDE) TABLET, FILM COATED [REBEL DISTRIBUTORS CORP] | 1 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | RELPAX (ELETRIPTAN HYDROBROMIDE) TABLET, FILM COATED [REBEL DISTRIBUTORS CORP] | 1 | |
| lactose | INACTIVE INGREDIENT | J2B2A4N98G | RELPAX (ELETRIPTAN HYDROBROMIDE) TABLET, FILM COATED [REBEL DISTRIBUTORS CORP] | 1 | |
| magnesium stearate | INACTIVE INGREDIENT | 70097M6I30 | RELPAX (ELETRIPTAN HYDROBROMIDE) TABLET, FILM COATED [REBEL DISTRIBUTORS CORP] | 1 | |
| titanium dioxide | INACTIVE INGREDIENT | 15FIX9V2JP | RELPAX (ELETRIPTAN HYDROBROMIDE) TABLET, FILM COATED [REBEL DISTRIBUTORS CORP] | 1 | |
| triacetin | INACTIVE INGREDIENT | XHX3C3X673 | RELPAX (ELETRIPTAN HYDROBROMIDE) TABLET, FILM COATED [REBEL DISTRIBUTORS CORP] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21695-871 | RELPAX (ELETRIPTAN HYDROBROMIDE) TABLET, FILM COATED [REBEL DISTRIBUTORS CORP] | 1 | Legacy NDC, 1 package rows | 20110104_6bb510c8-2ae2-4159-b4c6-0aec5e64b4c9.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 21695-871-40 | 21695087140 | 12 in 1 BLISTER PACK | Historical |