Hydrocodone Bitartrate and Acetaminophen
- Product NDC
- 60760-872
- 11-digit product format
- 607600872
- Labeler code
- 60760
- Product ID
- 60760-872_4f836f84-7a70-dc9e-e063-6294a90a3574
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrocodone Bitartrate and Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- ST. MARY'S MEDICAL PARK PHARMACY
- Application
- ANDA202214
- Marketing category
- ANDA
- Marketing start
- 2014-10-06
- Substance
- ACETAMINOPHEN; HYDROCODONE BITARTRATE
- Active strength
- 325; 10 mg/1; mg/1
- Pharmacologic classes
- Opioid Agonist [EPC], Opioid Agonists [MoA]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Hydrocodone Bitartrate and Acetaminophen
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACETAMINOPHEN | 325 mg/1 |
| HYDROCODONE BITARTRATE | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 362O9ITL9D, NO70W886KK |
| Rxcui | 856999 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 60760-872-30 | Hydrocodone Bitartrate and Acetaminophen | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | | 2 |
| 60760-872-60 | Hydrocodone Bitartrate and Acetaminophen | 60 in 1 BOTTLE, PLASTIC | TABLET | 60 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 60760-872-30 | 60760087230 | 30 TABLET in 1 BOTTLE, PLASTIC (60760-872-30) | 30 tablet | 2025-10-14 | No | No | Historical |
| 60760-872-60 | 60760087260 | 60 TABLET in 1 BOTTLE, PLASTIC (60760-872-60) | 60 tablet | 2025-10-14 | No | No | Historical |