Ketorolac Tromethamine
- Product NDC
- 21695-432
- 11-digit product format
- 216950432
- Labeler code
- 21695
- Product ID
- 21695-432_5914ef00-19b1-4e22-9ad3-2b62b455af9d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ketorolac Tromethamine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Rebel Distributors Corp
- Application
- ANDA074754
- Marketing category
- ANDA
- Marketing start
- 2010-04-20
- Marketing end
- 0000-00-00
- Substance
- KETOROLAC TROMETHAMINE
- Active strength
- 10 mg/1
- 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 |
|---|
| 21695-432-10 | Ketorolac Tromethamine | 10 in 1 BOTTLE | TABLET, FILM COATED | 10 | | 1 |
| 21695-432-12 | Ketorolac Tromethamine | 12 in 1 BOTTLE | TABLET, FILM COATED | 12 | | 1 |
| 21695-432-15 | Ketorolac Tromethamine | 15 in 1 BOTTLE | TABLET, FILM COATED | 15 | | 1 |
| 21695-432-20 | Ketorolac Tromethamine | 20 in 1 BOTTLE | TABLET, FILM COATED | 20 | | 1 |
| 21695-432-28 | Ketorolac Tromethamine | 28 in 1 BOTTLE | TABLET, FILM COATED | 28 | | 1 |
| 21695-432-30 | Ketorolac Tromethamine | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 1 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| KETOROLAC TROMETHAMINE | ACTIVE INGREDIENT | 4EVE5946BQ | KETOROLAC TROMETHAMINE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP] | 1 | |
| KETOROLAC TROMETHAMINE | ACTIVE MOIETY | 4EVE5946BQ | KETOROLAC TROMETHAMINE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | KETOROLAC TROMETHAMINE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP] | 1 | |
| HYDROXYPROPYL CELLULOSE | INACTIVE INGREDIENT | RFW2ET671P | KETOROLAC TROMETHAMINE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP] | 1 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | KETOROLAC TROMETHAMINE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP] | 1 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | KETOROLAC TROMETHAMINE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | KETOROLAC TROMETHAMINE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP] | 1 | |
| POLYETHYLENE GLYCOL | INACTIVE INGREDIENT | 3WJQ0SDW1A | KETOROLAC TROMETHAMINE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP] | 1 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | KETOROLAC TROMETHAMINE 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 |
|---|
| 21695-432 | KETOROLAC TROMETHAMINE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP] | 1 | Legacy NDC, 6 package rows | 20110917_5914ef00-19b1-4e22-9ad3-2b62b455af9d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 21695-432-10 | 21695043210 | 10 in 1 BOTTLE | Historical |
| 21695-432-12 | 21695043212 | 12 in 1 BOTTLE | Historical |
| 21695-432-15 | 21695043215 | 15 in 1 BOTTLE | Historical |
| 21695-432-20 | 21695043220 | 20 in 1 BOTTLE | Historical |
| 21695-432-28 | 21695043228 | 28 in 1 BOTTLE | Historical |
| 21695-432-30 | 21695043230 | 30 in 1 BOTTLE | Historical |