Adult Low Dose Aspirin
- Product NDC
- 0440-7135
- 11-digit product format
- 004407135
- Labeler code
- 0440
- Product ID
- 0440-7135_184e3741-fc36-42fa-ac4f-05cb36c8e2ed
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aspirin
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Liberty Pharmaceuticals, Inc.
- Application
- part343
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2007-01-12
- Marketing end
- 0000-00-00
- Substance
- ASPIRIN
- Active strength
- 81 mg/1
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 0440-7135-09 | Adult Low Dose Aspirin | 1 in 1 CARTON | TABLET, DELAYED RELEASE | 1 | | 1 |
| 0440-7135-90 | Adult Low Dose Aspirin | 90 in 1 BOTTLE, PLASTIC | TABLET, DELAYED RELEASE | 90 | | 1 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| ASPIRIN | ACTIVE INGREDIENT | R16CO5Y76E | ADULT LOW DOSE ASPIRIN (ASPIRIN) TABLET, DELAYED RELEASE [LIBERTY PHARMACEUTICALS, INC.] | 1 | |
| ASPIRIN | ACTIVE MOIETY | R16CO5Y76E | ADULT LOW DOSE ASPIRIN (ASPIRIN) TABLET, DELAYED RELEASE [LIBERTY PHARMACEUTICALS, INC.] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | ADULT LOW DOSE ASPIRIN (ASPIRIN) TABLET, DELAYED RELEASE [LIBERTY PHARMACEUTICALS, INC.] | 1 | |
| CROSCARMELLOSE SODIUM | INACTIVE INGREDIENT | M28OL1HH48 | ADULT LOW DOSE ASPIRIN (ASPIRIN) TABLET, DELAYED RELEASE [LIBERTY PHARMACEUTICALS, INC.] | 1 | |
| D&C YELLOW NO. 10 | INACTIVE INGREDIENT | 35SW5USQ3G | ADULT LOW DOSE ASPIRIN (ASPIRIN) TABLET, DELAYED RELEASE [LIBERTY PHARMACEUTICALS, INC.] | 1 | |
| FD&C YELLOW NO. 6 | INACTIVE INGREDIENT | H77VEI93A8 | ADULT LOW DOSE ASPIRIN (ASPIRIN) TABLET, DELAYED RELEASE [LIBERTY PHARMACEUTICALS, INC.] | 1 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | ADULT LOW DOSE ASPIRIN (ASPIRIN) TABLET, DELAYED RELEASE [LIBERTY PHARMACEUTICALS, INC.] | 1 | |
| METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A | INACTIVE INGREDIENT | NX76LV5T8J | ADULT LOW DOSE ASPIRIN (ASPIRIN) TABLET, DELAYED RELEASE [LIBERTY PHARMACEUTICALS, INC.] | 1 | |
| POLYETHYLENE GLYCOLS | INACTIVE INGREDIENT | 3WJQ0SDW1A | ADULT LOW DOSE ASPIRIN (ASPIRIN) TABLET, DELAYED RELEASE [LIBERTY PHARMACEUTICALS, INC.] | 1 | |
| SODIUM LAURYL SULFATE | INACTIVE INGREDIENT | 368GB5141J | ADULT LOW DOSE ASPIRIN (ASPIRIN) TABLET, DELAYED RELEASE [LIBERTY PHARMACEUTICALS, INC.] | 1 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | ADULT LOW DOSE ASPIRIN (ASPIRIN) TABLET, DELAYED RELEASE [LIBERTY PHARMACEUTICALS, INC.] | 1 | |
| STEARIC ACID | INACTIVE INGREDIENT | 4ELV7Z65AP | ADULT LOW DOSE ASPIRIN (ASPIRIN) TABLET, DELAYED RELEASE [LIBERTY PHARMACEUTICALS, INC.] | 1 | |
| TALC | INACTIVE INGREDIENT | 7SEV7J4R1U | ADULT LOW DOSE ASPIRIN (ASPIRIN) TABLET, DELAYED RELEASE [LIBERTY PHARMACEUTICALS, INC.] | 1 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | ADULT LOW DOSE ASPIRIN (ASPIRIN) TABLET, DELAYED RELEASE [LIBERTY PHARMACEUTICALS, INC.] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0440-7135 | ADULT LOW DOSE ASPIRIN (ASPIRIN) TABLET, DELAYED RELEASE [LIBERTY PHARMACEUTICALS, INC.] | 1 | Legacy NDC, 2 package rows | 20131204_b427f43b-6c79-4141-9709-8da63d198cc8.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 0440-7135-09 | 00440713509 | 1 in 1 CARTON | Historical |
| 0440-7135-90 | 00440713590 | 90 in 1 BOTTLE, PLASTIC | Historical |